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You searched for subject:(chromosomal microarray). Showing records 1 – 14 of 14 total matches.

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George Mason University

1. Tran, Khoa D. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .

Degree: 2014, George Mason University

 This thesis demonstrates the successful integration and application of chromosomal microarray analysis (CMA) and mutation-specific polymerase chain reaction (PCR) within 24 hours for the detection… (more)

Subjects/Keywords: Chromosomal Microarray Analysis; genetic disease mutation; fertility; PGD

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APA (6th Edition):

Tran, K. D. (2014). Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8995

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):

Tran, Khoa D. “Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .” 2014. Thesis, George Mason University. Accessed October 24, 2020. http://hdl.handle.net/1920/8995.

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

MLA Handbook (7th Edition):

Tran, Khoa D. “Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .” 2014. Web. 24 Oct 2020.

Vancouver:

Tran KD. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . [Internet] [Thesis]. George Mason University; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1920/8995.

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

Council of Science Editors:

Tran KD. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . [Thesis]. George Mason University; 2014. Available from: http://hdl.handle.net/1920/8995

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

2. Fonseca, Ana Carolina dos Santos. Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos.

Degree: Mestrado, Biologia (Genética), 2011, University of São Paulo

 Este estudo teve como objetivo identificar mecanismos pelos quais rearranjos cromossômicos aparentemente equilibrados possam estar associados de maneira causal a determinados quadros clínicos. Para isso… (more)

Subjects/Keywords: Alterações cromossômicas submicroscópicas; Balanced chromosomal rearrangements; Fluorescent in sit; Hibridação genômica em microarray; Hibridação in situ fluorescente; Rearranjos cromossômicos equilibrados; Submicroscopic chromosomal imbalances

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APA (6th Edition):

Fonseca, A. C. d. S. (2011). Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-20012012-153650/ ;

Chicago Manual of Style (16th Edition):

Fonseca, Ana Carolina dos Santos. “Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos.” 2011. Masters Thesis, University of São Paulo. Accessed October 24, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-20012012-153650/ ;.

MLA Handbook (7th Edition):

Fonseca, Ana Carolina dos Santos. “Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos.” 2011. Web. 24 Oct 2020.

Vancouver:

Fonseca ACdS. Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Oct 24]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-20012012-153650/ ;.

Council of Science Editors:

Fonseca ACdS. Caracterização de rearranjos cromossômicos aparentemente equilibrados associados a quadros clínicos. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-20012012-153650/ ;


Texas Medical Center

3. Durham, Leslie N. The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers.

Degree: MS, 2017, Texas Medical Center

Chromosomal microarray (CMA) assesses chromosome copy number variants (CNVs) missed by standard karyotyping. The American College of Obstetricians and Gynecologists (ACOG) recommends CMA for… (more)

Subjects/Keywords: Genetic counseling; prenatal; chromosomal microarray; barriers; practices; genetics; utilization; Genetics; Medical Genetics; Medicine and Health Sciences; Obstetrics and Gynecology

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APA (6th Edition):

Durham, L. N. (2017). The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/761

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):

Durham, Leslie N. “The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers.” 2017. Thesis, Texas Medical Center. Accessed October 24, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/761.

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

MLA Handbook (7th Edition):

Durham, Leslie N. “The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers.” 2017. Web. 24 Oct 2020.

Vancouver:

Durham LN. The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers. [Internet] [Thesis]. Texas Medical Center; 2017. [cited 2020 Oct 24]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/761.

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

Council of Science Editors:

Durham LN. The Utilization of Prenatal Microarray: A Survey of Current Genetic Counseling Practices and Barriers. [Thesis]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/761

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

4. Matsudate, Yoshihiro. Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断.

Degree: 博士(医学), 2017, Tokushima University / 徳島大学

Subjects/Keywords: nevoid basal cell carcinoma syndrome; targeted exome sequencing; chromosomal microarray; PTCH1

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Matsudate, Y. (2017). Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断. (Thesis). Tokushima University / 徳島大学. Retrieved from http://repo.lib.tokushima-u.ac.jp/110418

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):

Matsudate, Yoshihiro. “Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断.” 2017. Thesis, Tokushima University / 徳島大学. Accessed October 24, 2020. http://repo.lib.tokushima-u.ac.jp/110418.

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

MLA Handbook (7th Edition):

Matsudate, Yoshihiro. “Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断.” 2017. Web. 24 Oct 2020.

Vancouver:

Matsudate Y. Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断. [Internet] [Thesis]. Tokushima University / 徳島大学; 2017. [cited 2020 Oct 24]. Available from: http://repo.lib.tokushima-u.ac.jp/110418.

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

Council of Science Editors:

Matsudate Y. Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome : ターゲットエクソーム解析および染色体マイクロアレイ解析を用いた母斑性基底細胞癌症候群の遺伝子診断. [Thesis]. Tokushima University / 徳島大学; 2017. Available from: http://repo.lib.tokushima-u.ac.jp/110418

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

5. Mitrakos, Anastasios. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).

Degree: 2020, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Acute Lymphoblastic Leukemia (ALL) is a malignancy of the immature lymphoid cells mainly associated with numerical and structural chromosomal aberrations. The current standard for profiling… (more)

Subjects/Keywords: Συγκριτικός γενωμικός υβριδισμός σε μικροσυστοιχίες; Αιματολογικές κακοήθειες; Αλλαγές αριθμού αντιγράφων (CNVs); Χρωμοσωμική ανάλυση με μικροσυστοιχίες; Array comparative genomic hybridization (aCGH); Hematological malignancies; Copy number variants (CNVs); Chromosomal microarray analysis (CMA)

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APA (6th Edition):

Mitrakos, A. (2020). Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/47723

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):

Mitrakos, Anastasios. “Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).” 2020. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 24, 2020. http://hdl.handle.net/10442/hedi/47723.

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

MLA Handbook (7th Edition):

Mitrakos, Anastasios. “Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH).” 2020. Web. 24 Oct 2020.

Vancouver:

Mitrakos A. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10442/hedi/47723.

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

Council of Science Editors:

Mitrakos A. Μελέτη υπομικροσκοπικών γονιδιωματικών αλλοιώσεων σε ασθενείς με παιδιατρικές αιματολογικές κακοήθειες με τη μέθοδο του συγκριτικού γενωμικού υβριδισμού σε μικροσυστοιχίες (aCGH). [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2020. Available from: http://hdl.handle.net/10442/hedi/47723

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

6. 이, 형남. Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.

Degree: 2017, Ajou University

BACKGROUND: Chromosomal microarray (CMA) is a cytogenetic diagnostic test for chromosomal abnormalities in many diseases, which can provide the fast and accurate detection of copy-number… (more)

Subjects/Keywords: Chromosomal microarray (CMA); Copy-number variations (CNVs); Congenital anomaly; Developmental delay (DD); Intellectual disability (ID); 염색체 마이크로어레이; 복제수변이; 신경발달장애; 선천성 기형; 발달지연; 지적장애

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APA (6th Edition):

이, . (2017). Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829

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):

이, 형남. “Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.” 2017. Thesis, Ajou University. Accessed October 24, 2020. http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829.

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

MLA Handbook (7th Edition):

이, 형남. “Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea.” 2017. Web. 24 Oct 2020.

Vancouver:

이 . Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. [Internet] [Thesis]. Ajou University; 2017. [cited 2020 Oct 24]. Available from: http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829.

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

Council of Science Editors:

이 . Clinical application of chromosomal microarray as a first-tier chromosome aberration test for patients with developmental delay and intellectual disability in Korea. [Thesis]. Ajou University; 2017. Available from: http://repository.ajou.ac.kr/handle/201003/16464 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024829

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

7. Ευαγγελίδου-Μαυρογένη, Πάολα. Μοριακός καρυότυπος στην προγεννητική διάγνωση.

Degree: 2012, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

 Karyotyping has been the golden standard method for prenatal diagnosis fordecades, for the diagnosis of numerical and large structural abnormalities (<3-10Mb).With the introduction of array… (more)

Subjects/Keywords: Προγεννητική διάγνωση; Χρωμοσωμική εξέταση; Συγκριτικός γενομικός υβριδισμός; Ανευπλοειδίες; Πολυμορφισμοί; Prenatal diagnosis; Chromosomal analysis; Microarray comparative genomic hybridization (aCGH); Copy nymber variations (CNVs); Coincidental findings; Pathogenic findings; Aneuploidies; Polymorphisms

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APA (6th Edition):

Ευαγγελίδου-Μαυρογένη, . . (2012). Μοριακός καρυότυπος στην προγεννητική διάγνωση. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/36991

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):

Ευαγγελίδου-Μαυρογένη, Πάολα. “Μοριακός καρυότυπος στην προγεννητική διάγνωση.” 2012. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed October 24, 2020. http://hdl.handle.net/10442/hedi/36991.

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

MLA Handbook (7th Edition):

Ευαγγελίδου-Μαυρογένη, Πάολα. “Μοριακός καρυότυπος στην προγεννητική διάγνωση.” 2012. Web. 24 Oct 2020.

Vancouver:

Ευαγγελίδου-Μαυρογένη . Μοριακός καρυότυπος στην προγεννητική διάγνωση. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10442/hedi/36991.

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

Council of Science Editors:

Ευαγγελίδου-Μαυρογένη . Μοριακός καρυότυπος στην προγεννητική διάγνωση. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2012. Available from: http://hdl.handle.net/10442/hedi/36991

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

8. Choucair Alam, Nancy. Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability.

Degree: Docteur es, Biologie. Génétique, 2013, Aix-Marseille; Université Saint-Joseph (Beyrouth)

La déficience intellectuelle (DI) est une affection fréquente à causes multiples et souvent inconnues. Durant les 30 dernières années, l’examen utilisé pour l’exploration des anomalies… (more)

Subjects/Keywords: Déficience intellectuelle inexpliquée; Microremaniements (CNVs); Population libanaise; Hybridation sur puces à ADN; Classification des CNVs; Unexplained intellectual disability; Submicroscopic chromosomal imbalances (CNV); Lebanese population; Chromosomal microarray analysis (CMA); Classification of CNVs

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APA (6th Edition):

Choucair Alam, N. (2013). Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability. (Doctoral Dissertation). Aix-Marseille; Université Saint-Joseph (Beyrouth). Retrieved from http://www.theses.fr/2013AIXM5074

Chicago Manual of Style (16th Edition):

Choucair Alam, Nancy. “Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability.” 2013. Doctoral Dissertation, Aix-Marseille; Université Saint-Joseph (Beyrouth). Accessed October 24, 2020. http://www.theses.fr/2013AIXM5074.

MLA Handbook (7th Edition):

Choucair Alam, Nancy. “Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability.” 2013. Web. 24 Oct 2020.

Vancouver:

Choucair Alam N. Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability. [Internet] [Doctoral dissertation]. Aix-Marseille; Université Saint-Joseph (Beyrouth); 2013. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2013AIXM5074.

Council of Science Editors:

Choucair Alam N. Etude par puce à ADN d'une cohorte de 185 patients libanais atteints de déficience intellectuelle inexpliquée : Chromosomal microarray analysis of a cohort of 185 Lebanese patients with unexplained intellectual disability. [Doctoral Dissertation]. Aix-Marseille; Université Saint-Joseph (Beyrouth); 2013. Available from: http://www.theses.fr/2013AIXM5074

9. Goodman, Corey William. Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories.

Degree: MS, Electrical and Computer Engineering, 2012, University of Iowa

  Many disorders found in humans are caused by abnormalities in DNA. Genetic testing of DNA provides a way for clinicians to identify disease-causing mutations… (more)

Subjects/Keywords: calibration; chromosomal microarray; receiver operating characteristic; sensitivity; specificity; validation; Electrical and Computer Engineering

…40 xii 1 CHAPTER 1 INTRODUCTION Chromosomal microarray (CMA) is a broad term… …whole-genome chromosomal microarray platform or test kit. According to the ACMG, the… …validation of a clinical chromosomal microarray should be performed by testing a sufficiently large… …methods presented here can be applied to data from any chromosomal microarray with… …oligonucleotide probes, in this project the type of chromosomal microarray used was a comparative… 

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APA (6th Edition):

Goodman, C. W. (2012). Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories. (Masters Thesis). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/3301

Chicago Manual of Style (16th Edition):

Goodman, Corey William. “Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories.” 2012. Masters Thesis, University of Iowa. Accessed October 24, 2020. https://ir.uiowa.edu/etd/3301.

MLA Handbook (7th Edition):

Goodman, Corey William. “Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories.” 2012. Web. 24 Oct 2020.

Vancouver:

Goodman CW. Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories. [Internet] [Masters thesis]. University of Iowa; 2012. [cited 2020 Oct 24]. Available from: https://ir.uiowa.edu/etd/3301.

Council of Science Editors:

Goodman CW. Cost effective, computer-aided analytical performance evaluation of chromosomal microarrays for clinical laboratories. [Masters Thesis]. University of Iowa; 2012. Available from: https://ir.uiowa.edu/etd/3301

10. Brun, Stéphanie. Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis.

Degree: Docteur es, Génétique, 2019, Bordeaux

 ObjectifLe diagnostic prénatal (DPN) a pour but de détecter des pathologies foetales in utero. L’objectif de ce travail était de mettre au point et d’appliquer… (more)

Subjects/Keywords: Diagnostic Prenatal Non Invasif; Medecine foetale; CGH-Array; ADNlc; Retard de croissance intra uterin; Non Invasive Prenatal Screening; Fetal fraction; Array-CGH; IUGR intra uterin growth restriction; Prenatal diagnosis; Semiconductor sequencing; Trisomy; Chromosomal Microarray Analysis

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APA (6th Edition):

Brun, S. (2019). Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2019BORD0184

Chicago Manual of Style (16th Edition):

Brun, Stéphanie. “Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis.” 2019. Doctoral Dissertation, Bordeaux. Accessed October 24, 2020. http://www.theses.fr/2019BORD0184.

MLA Handbook (7th Edition):

Brun, Stéphanie. “Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis.” 2019. Web. 24 Oct 2020.

Vancouver:

Brun S. Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis. [Internet] [Doctoral dissertation]. Bordeaux; 2019. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2019BORD0184.

Council of Science Editors:

Brun S. Techniques d'exploration chromosomique en prénatal : mises au point et applications : Technical development and applications of the chromosomal exploration technics in prenatal diagnosis. [Doctoral Dissertation]. Bordeaux; 2019. Available from: http://www.theses.fr/2019BORD0184


University of Sydney

11. Mohamed Yousoof, Saira Bahnu. Genomic and functional approaches in identification and characterisation of novel eye disease genes .

Degree: 2013, University of Sydney

Subjects/Keywords: Eye anterior segment abnormalities; Translocations; Novel eye disease genes; Next-generation sequencing; Chromosomal microarray and zebrafish

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

APA (6th Edition):

Mohamed Yousoof, S. B. (2013). Genomic and functional approaches in identification and characterisation of novel eye disease genes . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/10055

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):

Mohamed Yousoof, Saira Bahnu. “Genomic and functional approaches in identification and characterisation of novel eye disease genes .” 2013. Thesis, University of Sydney. Accessed October 24, 2020. http://hdl.handle.net/2123/10055.

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

MLA Handbook (7th Edition):

Mohamed Yousoof, Saira Bahnu. “Genomic and functional approaches in identification and characterisation of novel eye disease genes .” 2013. Web. 24 Oct 2020.

Vancouver:

Mohamed Yousoof SB. Genomic and functional approaches in identification and characterisation of novel eye disease genes . [Internet] [Thesis]. University of Sydney; 2013. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2123/10055.

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

Council of Science Editors:

Mohamed Yousoof SB. Genomic and functional approaches in identification and characterisation of novel eye disease genes . [Thesis]. University of Sydney; 2013. Available from: http://hdl.handle.net/2123/10055

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

12. Andrew, Erin H. Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist.

Degree: MS, Medicine: Genetic Counseling, 2017, University of Cincinnati

Chromosomal microarray analysis (CMA) is currently the first-tier diagnostic test recommended for children with undiagnosed intellectual disabilities. Long ordered by geneticists, CMAs are now increasingly… (more)

Subjects/Keywords: Genetics; chromosomal microarray; parental experience; intellectual disability; developmental delay; diagnostic odyssey; genetic counseling

…disabilities is chromosomal microarray analysis (CMA) (Manning et al., 2010; Miller et… …genome to detect chromosomal abnormalities such as copy number variants (CNVs) which… …the test results make sense to you?” and “What do you understand the microarray results to… …chromosomal test is—I don’t feel like my need for information was ever really satisfied as far as… 

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):

Andrew, E. H. (2017). Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491305824301482

Chicago Manual of Style (16th Edition):

Andrew, Erin H. “Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist.” 2017. Masters Thesis, University of Cincinnati. Accessed October 24, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491305824301482.

MLA Handbook (7th Edition):

Andrew, Erin H. “Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist.” 2017. Web. 24 Oct 2020.

Vancouver:

Andrew EH. Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist. [Internet] [Masters thesis]. University of Cincinnati; 2017. [cited 2020 Oct 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491305824301482.

Council of Science Editors:

Andrew EH. Parental Experiences When CMA is Ordered by a Geneticist vs. Non-geneticist. [Masters Thesis]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1491305824301482


Universitetet i Tromsø

13. Winther, Alise Marie. Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping .

Degree: 2019, Universitetet i Tromsø

 Abstract Background: In prenatal diagnosis, chromosomal microarray analysis (CMA) has not yet fully replaced conventional karyotyping. As CMA is able to detect smaller genomic imbalances… (more)

Subjects/Keywords: Prenatal diagnosis; chromosomal microarray analysis; Genetics; VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical genetics: 714; VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714

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

APA (6th Edition):

Winther, A. M. (2019). Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping . (Masters Thesis). Universitetet i Tromsø. Retrieved from http://hdl.handle.net/10037/15743

Chicago Manual of Style (16th Edition):

Winther, Alise Marie. “Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping .” 2019. Masters Thesis, Universitetet i Tromsø. Accessed October 24, 2020. http://hdl.handle.net/10037/15743.

MLA Handbook (7th Edition):

Winther, Alise Marie. “Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping .” 2019. Web. 24 Oct 2020.

Vancouver:

Winther AM. Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping . [Internet] [Masters thesis]. Universitetet i Tromsø 2019. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10037/15743.

Council of Science Editors:

Winther AM. Chromosomal microarray in prenatal diagnosis - replacing traditional karyotyping . [Masters Thesis]. Universitetet i Tromsø 2019. Available from: http://hdl.handle.net/10037/15743

14. Serra Juhé, Clara, 1984-. Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling.

Degree: Departament de Ciències Experimentals i de la Salut, 2012, Universitat Pompeu Fabra

 Els mecanismes causants de les malformacions congènites són poc coneguts malgrat l’elevada incidència d’aquestes patologies, que afecten el 2-3% de recent nascuts. Un coneixement més… (more)

Subjects/Keywords: Malformacions congènites; Malformacions cardíaques congènites; Epigenètica; Variacions en número de còpia (CNV); Mutacions puntuals; Assessorament genètic; Análisis cromosòmica en micromatrius; Seqüenciació d’exoma; Metilació del DNA; Congenital malformations; Congenital heart defects; Epigenetics; Copy number variation (CNV); Point mutations; Genetic counseling; Chromosomal microarray analysis; Exome sequencing; DNA methylation; 575

…of the application of new molecular techniques, such as chromosomal microarray analysis… …69 Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis… …CMA (Chromosomal microarray analysis, including aCGH as well as SNP arrays) has… …and abnormality detection rates ................ 75 Table 2 Chromosomal alterations… …identified...................................................... 77 Table 3 Chromosomal… 

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

APA (6th Edition):

Serra Juhé, Clara, 1. (2012). Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/96194

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):

Serra Juhé, Clara, 1984-. “Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling.” 2012. Thesis, Universitat Pompeu Fabra. Accessed October 24, 2020. http://hdl.handle.net/10803/96194.

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

MLA Handbook (7th Edition):

Serra Juhé, Clara, 1984-. “Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling.” 2012. Web. 24 Oct 2020.

Vancouver:

Serra Juhé, Clara 1. Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling. [Internet] [Thesis]. Universitat Pompeu Fabra; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10803/96194.

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

Council of Science Editors:

Serra Juhé, Clara 1. Genetic, genomic and epigenetic alterations in congenital malformations : implications in genetic counseling. [Thesis]. Universitat Pompeu Fabra; 2012. Available from: http://hdl.handle.net/10803/96194

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

.