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You searched for subject:(SNP array). Showing records 1 – 29 of 29 total matches.

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University of Arizona

1. Quinto Cortes, Consuelo Dayzu. Inferring Demographic History of Admixed Human Populations with SNP Array Data .

Degree: 2016, University of Arizona

 The demographic history of human populations, both archaic and modern, have been the focus of extensive research. Earlier studies were based on a small number… (more)

Subjects/Keywords: Genetics; Inference; Population; SNP Array; Genetics; Demography

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APA (6th Edition):

Quinto Cortes, C. D. (2016). Inferring Demographic History of Admixed Human Populations with SNP Array Data . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/621870

Chicago Manual of Style (16th Edition):

Quinto Cortes, Consuelo Dayzu. “Inferring Demographic History of Admixed Human Populations with SNP Array Data .” 2016. Doctoral Dissertation, University of Arizona. Accessed October 31, 2020. http://hdl.handle.net/10150/621870.

MLA Handbook (7th Edition):

Quinto Cortes, Consuelo Dayzu. “Inferring Demographic History of Admixed Human Populations with SNP Array Data .” 2016. Web. 31 Oct 2020.

Vancouver:

Quinto Cortes CD. Inferring Demographic History of Admixed Human Populations with SNP Array Data . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10150/621870.

Council of Science Editors:

Quinto Cortes CD. Inferring Demographic History of Admixed Human Populations with SNP Array Data . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/621870


University of Gothenburg / Göteborgs Universitet

2. Kryh, Hanna. Molecular characterization of neuroblastoma tumors - a basis for personalized medicine.

Degree: 2012, University of Gothenburg / Göteborgs Universitet

 Neuroblastoma is a very heterogeneous tumor, with a clinical course ranging from spontaneous regression to aggressive tumor growth. A proper stratification of the patients into… (more)

Subjects/Keywords: Neuroblastoma; Cancer; Tumor; SNP-array; Micro array; DNA copy number

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APA (6th Edition):

Kryh, H. (2012). Molecular characterization of neuroblastoma tumors - a basis for personalized medicine. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/28956

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kryh, Hanna. “Molecular characterization of neuroblastoma tumors - a basis for personalized medicine.” 2012. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 31, 2020. http://hdl.handle.net/2077/28956.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kryh, Hanna. “Molecular characterization of neuroblastoma tumors - a basis for personalized medicine.” 2012. Web. 31 Oct 2020.

Vancouver:

Kryh H. Molecular characterization of neuroblastoma tumors - a basis for personalized medicine. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2077/28956.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kryh H. Molecular characterization of neuroblastoma tumors - a basis for personalized medicine. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2012. Available from: http://hdl.handle.net/2077/28956

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Lund

3. Lilljebjörn, Henrik. Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia.

Degree: 2011, University of Lund

 The t(12;21) translocation generates the ETV6/RUNX1 fusion gene, present in 25% of childhood acute lymphoblastic leukemia. This fusion gene is important for leukemia development but… (more)

Subjects/Keywords: Medical Genetics; SNP array; array CGH; ETV6/RUNX1-positive ALL; childhood ALL; exome sequencing

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APA (6th Edition):

Lilljebjörn, H. (2011). Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1787221 ; https://portal.research.lu.se/ws/files/3214386/1787229.pdf

Chicago Manual of Style (16th Edition):

Lilljebjörn, Henrik. “Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia.” 2011. Doctoral Dissertation, University of Lund. Accessed October 31, 2020. https://lup.lub.lu.se/record/1787221 ; https://portal.research.lu.se/ws/files/3214386/1787229.pdf.

MLA Handbook (7th Edition):

Lilljebjörn, Henrik. “Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia.” 2011. Web. 31 Oct 2020.

Vancouver:

Lilljebjörn H. Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia. [Internet] [Doctoral dissertation]. University of Lund; 2011. [cited 2020 Oct 31]. Available from: https://lup.lub.lu.se/record/1787221 ; https://portal.research.lu.se/ws/files/3214386/1787229.pdf.

Council of Science Editors:

Lilljebjörn H. Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia. [Doctoral Dissertation]. University of Lund; 2011. Available from: https://lup.lub.lu.se/record/1787221 ; https://portal.research.lu.se/ws/files/3214386/1787229.pdf


Texas A&M University

4. Fang, Erica. Molecular Studies in Horses with SRY-Positive XY Sex Reversal.

Degree: MS, Genetics, 2012, Texas A&M University

 Sex determination in mammals is regulated by the sex-determining region on the Y chromosome (SRY); the presence of SRY activates the male developmental pathway and… (more)

Subjects/Keywords: Horses; SRY; Sex Reversal; SNP analysis; array comparative genomic hybridization

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APA (6th Edition):

Fang, E. (2012). Molecular Studies in Horses with SRY-Positive XY Sex Reversal. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10580

Chicago Manual of Style (16th Edition):

Fang, Erica. “Molecular Studies in Horses with SRY-Positive XY Sex Reversal.” 2012. Masters Thesis, Texas A&M University. Accessed October 31, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10580.

MLA Handbook (7th Edition):

Fang, Erica. “Molecular Studies in Horses with SRY-Positive XY Sex Reversal.” 2012. Web. 31 Oct 2020.

Vancouver:

Fang E. Molecular Studies in Horses with SRY-Positive XY Sex Reversal. [Internet] [Masters thesis]. Texas A&M University; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10580.

Council of Science Editors:

Fang E. Molecular Studies in Horses with SRY-Positive XY Sex Reversal. [Masters Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10580

5. Romano, Alessandra. High resolution molecular karyotyping and proteomic analysis in hematological malignancies.

Degree: 2011, Università degli Studi di Catania

Il presente lavoro di tesi ha applicato i risultati della genomica funzionale in termini traslazionali a due neoplasie ematologiche: le sindromi mielodislastiche (MDS), e il… (more)

Subjects/Keywords: SNP arrays; Myelodysplasia; RPMA-Reverse Phase Micro Array; Multiple myeloma

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APA (6th Edition):

Romano, A. (2011). High resolution molecular karyotyping and proteomic analysis in hematological malignancies. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/96

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Romano, Alessandra. “High resolution molecular karyotyping and proteomic analysis in hematological malignancies.” 2011. Thesis, Università degli Studi di Catania. Accessed October 31, 2020. http://hdl.handle.net/10761/96.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Romano, Alessandra. “High resolution molecular karyotyping and proteomic analysis in hematological malignancies.” 2011. Web. 31 Oct 2020.

Vancouver:

Romano A. High resolution molecular karyotyping and proteomic analysis in hematological malignancies. [Internet] [Thesis]. Università degli Studi di Catania; 2011. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10761/96.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Romano A. High resolution molecular karyotyping and proteomic analysis in hematological malignancies. [Thesis]. Università degli Studi di Catania; 2011. Available from: http://hdl.handle.net/10761/96

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Georgia

6. Clevenger, Josh Paul. Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance.

Degree: 2017, University of Georgia

 Aflatoxin is a highly carcinogenic mycotoxin produced by Aspergillus spp that contaminates peanuts (Arachis hypogaea) pre- and post-harvest. Understanding the interaction between peanut and fungus,… (more)

Subjects/Keywords: Arachis; peanut; aflatoxin; Aspergillus; transcriptome; homeolog; alternative splicing; SNP; SWEEP; genetic diversity; SNP array; pre-harvest aflatoxin contamination (PAC)

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APA (6th Edition):

Clevenger, J. P. (2017). Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/36688

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Clevenger, Josh Paul. “Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance.” 2017. Thesis, University of Georgia. Accessed October 31, 2020. http://hdl.handle.net/10724/36688.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Clevenger, Josh Paul. “Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance.” 2017. Web. 31 Oct 2020.

Vancouver:

Clevenger JP. Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance. [Internet] [Thesis]. University of Georgia; 2017. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10724/36688.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Clevenger JP. Development of genomics resources for arachis hypogaea and profiling the genetic regulation of pre-harvest aflatoxin resistance. [Thesis]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/36688

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

7. Dubois, Julie. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2012, Université de Bordeaux Segalen

Les syndromes myélodysplasiques (SMD) sont des hémopathies myéloïdes clonales évoluant vers une leucémie aiguë (LA). Les SMD et LA secondaires, survenant après traitement par chimiothérapie… (more)

Subjects/Keywords: SMD/LA secondaires; Polymorphismes génétiques SNP; Puce « à façon » de génotypage; Therapy-related MDS/AML; Single Nucleotide Polymorphisms (SNP); Custom-made SNP array

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APA (6th Edition):

Dubois, J. (2012). Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2012BOR21990

Chicago Manual of Style (16th Edition):

Dubois, Julie. “Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.” 2012. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed October 31, 2020. http://www.theses.fr/2012BOR21990.

MLA Handbook (7th Edition):

Dubois, Julie. “Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility.” 2012. Web. 31 Oct 2020.

Vancouver:

Dubois J. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2012. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2012BOR21990.

Council of Science Editors:

Dubois J. Syndromes myélodysplasiques de novo et secondaires à un traitement anti-cancéreux : recherche de marqueurs génétiques de susceptibilité individuelle : Therapy-related myelodysplastic syndromes : identification of genetic markers of individual susceptibility. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2012. Available from: http://www.theses.fr/2012BOR21990


Texas A&M University

8. Smith, Schuyler. Molecular Characterization of the Texas Maize Breeding Program.

Degree: MS, Plant Breeding, 2015, Texas A&M University

 The Texas maize breeding program at Texas A&M University has been unique among breeding programs for the incorporation of a wealth of germplasm from a… (more)

Subjects/Keywords: Molecular characterization; diversity study; subtropical; tropical; maize; SNP array; Texas; PCoA; STRUCTURE

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APA (6th Edition):

Smith, S. (2015). Molecular Characterization of the Texas Maize Breeding Program. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155199

Chicago Manual of Style (16th Edition):

Smith, Schuyler. “Molecular Characterization of the Texas Maize Breeding Program.” 2015. Masters Thesis, Texas A&M University. Accessed October 31, 2020. http://hdl.handle.net/1969.1/155199.

MLA Handbook (7th Edition):

Smith, Schuyler. “Molecular Characterization of the Texas Maize Breeding Program.” 2015. Web. 31 Oct 2020.

Vancouver:

Smith S. Molecular Characterization of the Texas Maize Breeding Program. [Internet] [Masters thesis]. Texas A&M University; 2015. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1969.1/155199.

Council of Science Editors:

Smith S. Molecular Characterization of the Texas Maize Breeding Program. [Masters Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155199

9. Bubien, Virginie. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.

Degree: Docteur es, Génétique, 2016, Bordeaux

5 à 10% des cancers du sein sont héréditaires mais parmi ceux-ci seulement la moitié est expliquée par une altération constitutionnelle d’un gène de prédisposition… (more)

Subjects/Keywords: Cancer du sein familial; ATM; Puces SNP; NGS; Risque de cancer du sein; Familial breast cancer; ATM; SNP array; NGS; Breast cancer risk

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APA (6th Edition):

Bubien, V. (2016). Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0393

Chicago Manual of Style (16th Edition):

Bubien, Virginie. “Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.” 2016. Doctoral Dissertation, Bordeaux. Accessed October 31, 2020. http://www.theses.fr/2016BORD0393.

MLA Handbook (7th Edition):

Bubien, Virginie. “Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.” 2016. Web. 31 Oct 2020.

Vancouver:

Bubien V. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2016BORD0393.

Council of Science Editors:

Bubien V. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0393

10. 菅, 安寿子. 子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas.

Degree: 医学博士, 2015, Iwate Medical University / 岩手医科大学

2015

Subjects/Keywords: CIMP; CNV; endometrial endometrioid adenocarcinoma; MSI; PTEN; SNP array

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APA (6th Edition):

菅, . (2015). 子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas. (Thesis). Iwate Medical University / 岩手医科大学. Retrieved from http://id.nii.ac.jp/1181/00005432/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

菅, 安寿子. “子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas.” 2015. Thesis, Iwate Medical University / 岩手医科大学. Accessed October 31, 2020. http://id.nii.ac.jp/1181/00005432/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

菅, 安寿子. “子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas.” 2015. Web. 31 Oct 2020.

Vancouver:

菅 . 子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas. [Internet] [Thesis]. Iwate Medical University / 岩手医科大学; 2015. [cited 2020 Oct 31]. Available from: http://id.nii.ac.jp/1181/00005432/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

菅 . 子宮類内膜腺癌における分離腫瘍腺管を用いた分子解析 : Molecular analysis of isolated tumor glands from endometrial endometrioid adenocarcinomas. [Thesis]. Iwate Medical University / 岩手医科大学; 2015. Available from: http://id.nii.ac.jp/1181/00005432/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

11. Mattsson, Anna. Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array.

Degree: Biomedical Laboratory Science, 2011, Umeå University

Subjects/Keywords: SNP-array; chromosomes; copy number variants; leukemia; aberrations; 11q23

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APA (6th Edition):

Mattsson, A. (2011). Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array. (Thesis). Umeå University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-58641

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mattsson, Anna. “Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array.” 2011. Thesis, Umeå University. Accessed October 31, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-58641.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mattsson, Anna. “Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array.” 2011. Web. 31 Oct 2020.

Vancouver:

Mattsson A. Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array. [Internet] [Thesis]. Umeå University; 2011. [cited 2020 Oct 31]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-58641.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mattsson A. Difference in copy number variants in peripheral blood and bone marrow detected by SNP-array. [Thesis]. Umeå University; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-58641

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

12. Capizzi, Carmela. Novel genomic technologies and molecular diagnostics in Colorectal Cancer.

Degree: 2012, Università degli Studi di Catania

 Cancer is a disease of the genome that is characterized by substantial variability in the clinical course and response to therapies. Colorectal cancer (CRC) is… (more)

Subjects/Keywords: Area 06 - Scienze mediche; Colorectal cancer, SNP-array, Bioinformatics, Microsatellite Instability, Chromosomal Instability, Copy Neutral Loss of Heterozygosity, Copy Number Abnormalities

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APA (6th Edition):

Capizzi, C. (2012). Novel genomic technologies and molecular diagnostics in Colorectal Cancer. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/919

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Capizzi, Carmela. “Novel genomic technologies and molecular diagnostics in Colorectal Cancer.” 2012. Thesis, Università degli Studi di Catania. Accessed October 31, 2020. http://hdl.handle.net/10761/919.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Capizzi, Carmela. “Novel genomic technologies and molecular diagnostics in Colorectal Cancer.” 2012. Web. 31 Oct 2020.

Vancouver:

Capizzi C. Novel genomic technologies and molecular diagnostics in Colorectal Cancer. [Internet] [Thesis]. Università degli Studi di Catania; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10761/919.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Capizzi C. Novel genomic technologies and molecular diagnostics in Colorectal Cancer. [Thesis]. Università degli Studi di Catania; 2012. Available from: http://hdl.handle.net/10761/919

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

13. Kohl, Ilana. Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento.

Degree: PhD, Biologia (Genética), 2010, University of São Paulo

Obesidade sindrômica é definida como a obesidade ocorrendo em conjunto com várias características clínicas distintas, associadas a retardo mental. A forma sindrômica mais freqüente é… (more)

Subjects/Keywords: Atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado; Behavior disorders; Developmental delay and / or learning difficulties; Distúrbios de comportamento; MLPA; MLPA; Obesidade e/ou Hiperfagia; Obesity and/ or hyperphagia; SNP-Array; SNP-Array

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APA (6th Edition):

Kohl, I. (2010). Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-07102010-134828/ ;

Chicago Manual of Style (16th Edition):

Kohl, Ilana. “Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento.” 2010. Doctoral Dissertation, University of São Paulo. Accessed October 31, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-07102010-134828/ ;.

MLA Handbook (7th Edition):

Kohl, Ilana. “Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento.” 2010. Web. 31 Oct 2020.

Vancouver:

Kohl I. Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Oct 31]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-07102010-134828/ ;.

Council of Science Editors:

Kohl I. Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-07102010-134828/ ;

14. Gijsbers, Antonia Christina Johanna. High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics.

Degree: 2010, Department of Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Conventional karyotyping has been used as the standard cytogenetic technique since the 1970s. With conventional karyotyping one can detect aberrations larger than 5 – 10… (more)

Subjects/Keywords: Copy number variation; Mental retardation; SNP array; Copy number variation; Mental retardation; SNP array

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gijsbers, A. C. J. (2010). High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics. (Doctoral Dissertation). Department of Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/16187

Chicago Manual of Style (16th Edition):

Gijsbers, Antonia Christina Johanna. “High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics.” 2010. Doctoral Dissertation, Department of Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed October 31, 2020. http://hdl.handle.net/1887/16187.

MLA Handbook (7th Edition):

Gijsbers, Antonia Christina Johanna. “High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics.” 2010. Web. 31 Oct 2020.

Vancouver:

Gijsbers ACJ. High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics. [Internet] [Doctoral dissertation]. Department of Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2010. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1887/16187.

Council of Science Editors:

Gijsbers ACJ. High-resolution karyotyping by oligonucleotide microarrays: the next revolution in cytogenetics. [Doctoral Dissertation]. Department of Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2010. Available from: http://hdl.handle.net/1887/16187

15. Avinash M. V. Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;.

Degree: 2013, University of Mysore

newline

Advisors/Committee Members: Ramachandra, N. B..

Subjects/Keywords: Genetics; Genetic Variation; Human cytogenetics; Human genetics; Human genome; SNP and CNV Array

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APA (6th Edition):

V., A. M. (2013). Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;. (Thesis). University of Mysore. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37083

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

V., Avinash M.. “Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;.” 2013. Thesis, University of Mysore. Accessed October 31, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/37083.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

V., Avinash M.. “Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;.” 2013. Web. 31 Oct 2020.

Vancouver:

V. AM. Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;. [Internet] [Thesis]. University of Mysore; 2013. [cited 2020 Oct 31]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37083.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

V. AM. Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero;. [Thesis]. University of Mysore; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37083

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

16. Ocheya, Silvano Assanga. Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits.

Degree: PhD, Plant Breeding, 2016, Texas A&M University

 Defining genetic architecture of complex traits is a fundamental step towards marker-assisted selection. The objective of this study was to use a saturated genetic map… (more)

Subjects/Keywords: Quantitative trait loci; genetic mapping; end-use quality; multi-trait QTL analysis; QTL-by-environment interaction; Single nucleotide polymorphism; 90K SNP array

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ocheya, S. A. (2016). Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/157942

Chicago Manual of Style (16th Edition):

Ocheya, Silvano Assanga. “Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 31, 2020. http://hdl.handle.net/1969.1/157942.

MLA Handbook (7th Edition):

Ocheya, Silvano Assanga. “Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits.” 2016. Web. 31 Oct 2020.

Vancouver:

Ocheya SA. Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1969.1/157942.

Council of Science Editors:

Ocheya SA. Genetic Mapping and Phenotypic Characterization of Wheat for Yield, Yield Components and Agronomic Traits. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/157942


University of Western Ontario

17. Patel, Nisha. A bioinformatics analysis of contributors to false discovery for a mouse genotyping array.

Degree: 2018, University of Western Ontario

 Microarray experiments employing massively-parallel hybridization are valuable for the study of genetic variation, however, errors during hybridization and limitations of single-species design must be considered… (more)

Subjects/Keywords: Mouse Diversity Genotyping Array; Mus musculus; hybridization; microarray probes; copy number variants; single nucleotide polymorphism; SNP genotyping; cross-species hybridization; naked mole-rat; Biology; Genetics and Genomics

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APA (6th Edition):

Patel, N. (2018). A bioinformatics analysis of contributors to false discovery for a mouse genotyping array. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5647

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Patel, Nisha. “A bioinformatics analysis of contributors to false discovery for a mouse genotyping array.” 2018. Thesis, University of Western Ontario. Accessed October 31, 2020. https://ir.lib.uwo.ca/etd/5647.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Patel, Nisha. “A bioinformatics analysis of contributors to false discovery for a mouse genotyping array.” 2018. Web. 31 Oct 2020.

Vancouver:

Patel N. A bioinformatics analysis of contributors to false discovery for a mouse genotyping array. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2020 Oct 31]. Available from: https://ir.lib.uwo.ca/etd/5647.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Patel N. A bioinformatics analysis of contributors to false discovery for a mouse genotyping array. [Thesis]. University of Western Ontario; 2018. Available from: https://ir.lib.uwo.ca/etd/5647

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

18. Kowgier, Matthew. Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays.

Degree: 2012, University of Toronto

DNA copy number variations (CNVs), which involve the deletion or duplication of subchromosomal segments of the genome, have become a focus of genetics research. This… (more)

Subjects/Keywords: DNA copy number; Bayesian HMM; SNP array; 0308; 0715

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Sample image

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kowgier, M. (2012). Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32794

Chicago Manual of Style (16th Edition):

Kowgier, Matthew. “Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays.” 2012. Doctoral Dissertation, University of Toronto. Accessed October 31, 2020. http://hdl.handle.net/1807/32794.

MLA Handbook (7th Edition):

Kowgier, Matthew. “Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays.” 2012. Web. 31 Oct 2020.

Vancouver:

Kowgier M. Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1807/32794.

Council of Science Editors:

Kowgier M. Bayesian Hidden Markov Models for finding DNA Copy Number Changes from SNP Genotyping Arrays. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32794

19. Fariña Sarasqueta, Aranzazu. Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer.

Degree: 2012, Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Colon cancer is the third most frequent malignancy in the Western world. Average 5 year-survival is around 70% and depends on the stage of the… (more)

Subjects/Keywords: Colon cancer; Gene mutation; Pharmacogenetics; Predictive markers; Prognostic markers; SNP array; Survival; Colon cancer; Gene mutation; Pharmacogenetics; Predictive markers; Prognostic markers; SNP array; Survival

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APA (6th Edition):

Fariña Sarasqueta, A. (2012). Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer. (Doctoral Dissertation). Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/19032

Chicago Manual of Style (16th Edition):

Fariña Sarasqueta, Aranzazu. “Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer.” 2012. Doctoral Dissertation, Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed October 31, 2020. http://hdl.handle.net/1887/19032.

MLA Handbook (7th Edition):

Fariña Sarasqueta, Aranzazu. “Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer.” 2012. Web. 31 Oct 2020.

Vancouver:

Fariña Sarasqueta A. Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer. [Internet] [Doctoral dissertation]. Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2012. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1887/19032.

Council of Science Editors:

Fariña Sarasqueta A. Molecular prognostic and predicitive markers of therapy response in sporadic colon cancer. [Doctoral Dissertation]. Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2012. Available from: http://hdl.handle.net/1887/19032

20. Lips, Esther Hélène. Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis.

Degree: 2008, Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Total mesorectal excision (TME) is the standard treatment for rectal cancer, while transanal endoscopic microsurgery (TEM) is a recently introduced surgical approach for the treatment… (more)

Subjects/Keywords: Rectal Cancer; Adenoma; Genomics; SNP Array; Gene expression; Analysis; Microarray; FFPE; Rectal Cancer; Adenoma; Genomics; SNP Array; Gene expression; Analysis; Microarray; FFPE

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APA (6th Edition):

Lips, E. H. (2008). Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis. (Doctoral Dissertation). Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/12962

Chicago Manual of Style (16th Edition):

Lips, Esther Hélène. “Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis.” 2008. Doctoral Dissertation, Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed October 31, 2020. http://hdl.handle.net/1887/12962.

MLA Handbook (7th Edition):

Lips, Esther Hélène. “Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis.” 2008. Web. 31 Oct 2020.

Vancouver:

Lips EH. Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis. [Internet] [Doctoral dissertation]. Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1887/12962.

Council of Science Editors:

Lips EH. Molecular discrimination of sessile rectal adenomas from carcinomas for a better treatment choice: integration of chromosomal instability patterns and expression array analysis. [Doctoral Dissertation]. Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. Available from: http://hdl.handle.net/1887/12962


University of Lund

21. Davidsson, Josef. Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia.

Degree: 2009, University of Lund

 The aim of this thesis was to analyze the genetic and epigenetic characteristics of pediatric high hyperdiploid acute lymphoblastic leukemia (HeH ALL), the most common… (more)

Subjects/Keywords: Medical Genetics; high hyperdiploid ALL; children; chromosome aberration; methylation profiling; array CGH; relapse; SNP array; clonal relationship; dup(1q)

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APA (6th Edition):

Davidsson, J. (2009). Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1502508 ; https://portal.research.lu.se/ws/files/4311589/1502510.pdf

Chicago Manual of Style (16th Edition):

Davidsson, Josef. “Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia.” 2009. Doctoral Dissertation, University of Lund. Accessed October 31, 2020. https://lup.lub.lu.se/record/1502508 ; https://portal.research.lu.se/ws/files/4311589/1502510.pdf.

MLA Handbook (7th Edition):

Davidsson, Josef. “Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia.” 2009. Web. 31 Oct 2020.

Vancouver:

Davidsson J. Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia. [Internet] [Doctoral dissertation]. University of Lund; 2009. [cited 2020 Oct 31]. Available from: https://lup.lub.lu.se/record/1502508 ; https://portal.research.lu.se/ws/files/4311589/1502510.pdf.

Council of Science Editors:

Davidsson J. Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia. [Doctoral Dissertation]. University of Lund; 2009. Available from: https://lup.lub.lu.se/record/1502508 ; https://portal.research.lu.se/ws/files/4311589/1502510.pdf

22. Lalonde, Matthew Scott. HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination.

Degree: PhD, Biochemistry, 2009, Case Western Reserve University School of Graduate Studies

  Pathogen micro-evolution in the host organism creates many similar variants of the same pathogen, a quasispecies. Human immunodeficiency virus is one such pathogen which… (more)

Subjects/Keywords: Biochemistry; SNP; ligase; minority; polymorphisms; suspension array; Luminex; oligonucleotide; DNA mixtures; LDR; array; hybridization

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APA (6th Edition):

Lalonde, M. S. (2009). HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1244059520

Chicago Manual of Style (16th Edition):

Lalonde, Matthew Scott. “HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination.” 2009. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1244059520.

MLA Handbook (7th Edition):

Lalonde, Matthew Scott. “HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination.” 2009. Web. 31 Oct 2020.

Vancouver:

Lalonde MS. HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2009. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1244059520.

Council of Science Editors:

Lalonde MS. HIV Drug Resistance Polymorphism Analysis Using Ligase Discrimination. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1244059520

23. Duyvenvoorde, Hermine Agatha van. Genetic causes of growth disorders.

Degree: 2013, Departments of Pediatrics, Endocrinology and Metabolic Diseases, Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Growth in humans, primarily longitudinal growth, is a complex process which starts at conception and proceeds through various developmental stages, mainly controlled by genetic factors… (more)

Subjects/Keywords: GH; Growth; IGF-I; NPR2; Short stature; SNP array; Tall stature; , Whole exome sequencing; GH; Growth; IGF-I; NPR2; Short stature; SNP array; Tall stature; , Whole exome sequencing

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APA (6th Edition):

Duyvenvoorde, H. A. v. (2013). Genetic causes of growth disorders. (Doctoral Dissertation). Departments of Pediatrics, Endocrinology and Metabolic Diseases, Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/21013

Chicago Manual of Style (16th Edition):

Duyvenvoorde, Hermine Agatha van. “Genetic causes of growth disorders.” 2013. Doctoral Dissertation, Departments of Pediatrics, Endocrinology and Metabolic Diseases, Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed October 31, 2020. http://hdl.handle.net/1887/21013.

MLA Handbook (7th Edition):

Duyvenvoorde, Hermine Agatha van. “Genetic causes of growth disorders.” 2013. Web. 31 Oct 2020.

Vancouver:

Duyvenvoorde HAv. Genetic causes of growth disorders. [Internet] [Doctoral dissertation]. Departments of Pediatrics, Endocrinology and Metabolic Diseases, Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1887/21013.

Council of Science Editors:

Duyvenvoorde HAv. Genetic causes of growth disorders. [Doctoral Dissertation]. Departments of Pediatrics, Endocrinology and Metabolic Diseases, Clinical Genetics, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2013. Available from: http://hdl.handle.net/1887/21013

24. Oussalah, Abderrahim. Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2011, Université Henri Poincaré – Nancy I

Des études d'associations pangénomiques ont démontré une relation entre le taux plasmatique de la vitamine B12 et le polymorphisme du gène FUT2 (fucosyltransferase 2). Dans… (more)

Subjects/Keywords: Métabolisme des monocarbones; Vitamine B12; Helicobacter pylori; Fucosyltransférase 2; Fut2 461 g>; a; Homocystéine; Méta-analyse; Single nucleotide polymorphism; SNP array (Illumina); Superoxyde dismutase; Maladies inflammatoires chroniques de l'intestin; Maladie de Crohn; 572.58; 616.344

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APA (6th Edition):

Oussalah, A. (2011). Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2011NAN10088

Chicago Manual of Style (16th Edition):

Oussalah, Abderrahim. “Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease.” 2011. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed October 31, 2020. http://www.theses.fr/2011NAN10088.

MLA Handbook (7th Edition):

Oussalah, Abderrahim. “Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease.” 2011. Web. 31 Oct 2020.

Vancouver:

Oussalah A. Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2011. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2011NAN10088.

Council of Science Editors:

Oussalah A. Déterminants génétiques du métabolisme des monocarbones : approche gène candidat dans deux populations ambulatoires et étude d'association avec la maladie de Crohn : Genetic determinants of one carbon metabolism : candidate gene approach in two ambulatory populations and genome association study in patients with Crohn's disease. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2011. Available from: http://www.theses.fr/2011NAN10088


University of Lund

25. Hofvander, Jakob. Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas.

Degree: 2019, University of Lund

Subjects/Keywords: Medical and Health Sciences; Sarcomas; Gene fusion; tumor evolution; clonal heterogeneity; RNA-seq; WES; SNP-array

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APA (6th Edition):

Hofvander, J. (2019). Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/244313f3-8244-4377-b4c6-3d32579665ae ; https://portal.research.lu.se/ws/files/55729688/elektronisk_utan_manuskript.pdf

Chicago Manual of Style (16th Edition):

Hofvander, Jakob. “Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas.” 2019. Doctoral Dissertation, University of Lund. Accessed October 31, 2020. https://lup.lub.lu.se/record/244313f3-8244-4377-b4c6-3d32579665ae ; https://portal.research.lu.se/ws/files/55729688/elektronisk_utan_manuskript.pdf.

MLA Handbook (7th Edition):

Hofvander, Jakob. “Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas.” 2019. Web. 31 Oct 2020.

Vancouver:

Hofvander J. Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas. [Internet] [Doctoral dissertation]. University of Lund; 2019. [cited 2020 Oct 31]. Available from: https://lup.lub.lu.se/record/244313f3-8244-4377-b4c6-3d32579665ae ; https://portal.research.lu.se/ws/files/55729688/elektronisk_utan_manuskript.pdf.

Council of Science Editors:

Hofvander J. Massively Parallel Sequencing of Gene Fusion-Associated Sarcomas. [Doctoral Dissertation]. University of Lund; 2019. Available from: https://lup.lub.lu.se/record/244313f3-8244-4377-b4c6-3d32579665ae ; https://portal.research.lu.se/ws/files/55729688/elektronisk_utan_manuskript.pdf


University of Toronto

26. Machado, Jerry. The Molecular Characterization of Head and Neck Cancer in Young Patients.

Degree: 2010, University of Toronto

Head and neck squamous cell carcinomas (HNSCCs) most commonly develop in older patients (≥60 years of age) with a history of tobacco and alcohol use.… (more)

Subjects/Keywords: Head and Neck Cancer; Young Patients; Oral Cancer; Human Papillomavirus; SNP Array; Mismatch Repair; 0307

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APA (6th Edition):

Machado, J. (2010). The Molecular Characterization of Head and Neck Cancer in Young Patients. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/24818

Chicago Manual of Style (16th Edition):

Machado, Jerry. “The Molecular Characterization of Head and Neck Cancer in Young Patients.” 2010. Doctoral Dissertation, University of Toronto. Accessed October 31, 2020. http://hdl.handle.net/1807/24818.

MLA Handbook (7th Edition):

Machado, Jerry. “The Molecular Characterization of Head and Neck Cancer in Young Patients.” 2010. Web. 31 Oct 2020.

Vancouver:

Machado J. The Molecular Characterization of Head and Neck Cancer in Young Patients. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1807/24818.

Council of Science Editors:

Machado J. The Molecular Characterization of Head and Neck Cancer in Young Patients. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24818


University of New South Wales

27. Zarzour, Peter. Considerations for the genome-wide profiling of colorectal neoplasia.

Degree: Clinical School - Prince of Wales Hospital, 2015, University of New South Wales

 Recent technological advances have made possible the generation of whole genome sequences at high throughput and low cost. Recent studies have capitalised on these advances… (more)

Subjects/Keywords: Expression profile; Colorectal neoplasia; Genome-wide profiling; RNA-seq; Single sample; Biological variability; Technical variability; Normal human colonic expression profile; Gene-rank approach; Colonic stem cell; SNP array; Copy number alterations

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zarzour, P. (2015). Considerations for the genome-wide profiling of colorectal neoplasia. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54549 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35289/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Zarzour, Peter. “Considerations for the genome-wide profiling of colorectal neoplasia.” 2015. Doctoral Dissertation, University of New South Wales. Accessed October 31, 2020. http://handle.unsw.edu.au/1959.4/54549 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35289/SOURCE02?view=true.

MLA Handbook (7th Edition):

Zarzour, Peter. “Considerations for the genome-wide profiling of colorectal neoplasia.” 2015. Web. 31 Oct 2020.

Vancouver:

Zarzour P. Considerations for the genome-wide profiling of colorectal neoplasia. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2020 Oct 31]. Available from: http://handle.unsw.edu.au/1959.4/54549 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35289/SOURCE02?view=true.

Council of Science Editors:

Zarzour P. Considerations for the genome-wide profiling of colorectal neoplasia. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54549 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35289/SOURCE02?view=true

28. Puijenbroek, Marjo van. Molecular pathology of colorectal cancer predisposing syndromes.

Degree: 2008, Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Each year, approximately eleven thousand new colorectal cancer (CRC) patients are registered in the Netherlands. Half of these patients will eventually die of this disease.… (more)

Subjects/Keywords: Cancer predisposing syndromes; Lynch syndrome; MUTYH; KRAS; Immunohistochemistry; Microsatellite instability; Tissue microarray; Loss of heterozygosity; SNP array; Formalin-fixed paraffin-embedded tissue; Familial colorectal cancer; Cancer predisposing syndromes; Lynch syndrome; MUTYH; KRAS; Immunohistochemistry; Microsatellite instability; Tissue microarray; Loss of heterozygosity; SNP array; Formalin-fixed paraffin-embedded tissue; Familial colorectal cancer

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Puijenbroek, M. v. (2008). Molecular pathology of colorectal cancer predisposing syndromes. (Doctoral Dissertation). Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/13286

Chicago Manual of Style (16th Edition):

Puijenbroek, Marjo van. “Molecular pathology of colorectal cancer predisposing syndromes.” 2008. Doctoral Dissertation, Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed October 31, 2020. http://hdl.handle.net/1887/13286.

MLA Handbook (7th Edition):

Puijenbroek, Marjo van. “Molecular pathology of colorectal cancer predisposing syndromes.” 2008. Web. 31 Oct 2020.

Vancouver:

Puijenbroek Mv. Molecular pathology of colorectal cancer predisposing syndromes. [Internet] [Doctoral dissertation]. Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1887/13286.

Council of Science Editors:

Puijenbroek Mv. Molecular pathology of colorectal cancer predisposing syndromes. [Doctoral Dissertation]. Department of Pathology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2008. Available from: http://hdl.handle.net/1887/13286

29. Rajaei, Saideh. Genetic studies of children with mental retardation.

Degree: 2013, University of Gothenburg / Göteborgs Universitet

 Mental retardation (MR) is characterised by significant limitations in intellectual function and adaptive behaviour. It is estimated that MR affects up to 3% of the… (more)

Subjects/Keywords: Mental retardation; Rett syndrome,; RTT; early onset infantile RTT; MECP2; SMR; SNP array; copy number variations; CNV; MECP2 duplication syndrome

Page 1 Page 2

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rajaei, S. (2013). Genetic studies of children with mental retardation. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/31714

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rajaei, Saideh. “Genetic studies of children with mental retardation.” 2013. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 31, 2020. http://hdl.handle.net/2077/31714.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rajaei, Saideh. “Genetic studies of children with mental retardation.” 2013. Web. 31 Oct 2020.

Vancouver:

Rajaei S. Genetic studies of children with mental retardation. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2013. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2077/31714.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rajaei S. Genetic studies of children with mental retardation. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2013. Available from: http://hdl.handle.net/2077/31714

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.