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You searched for subject:(molecular karyotyping). Showing records 1 – 6 of 6 total matches.

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1. Syrmou, Areti. Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο.

Degree: 2018, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 The definition of congenital anomalies refers to any structural, functional, metabolic disorder that occurs in the fetus during prenatal development and becomes evident either at… (more)

Subjects/Keywords: Μοριακός καρυότυπος; Συγγενείς ανωμαλίες; Molecular karyotyping; Congenital abnormalities

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

APA (6th Edition):

Syrmou, A. (2018). Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42449

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):

Syrmou, Areti. “Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο.” 2018. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 29, 2020. http://hdl.handle.net/10442/hedi/42449.

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

MLA Handbook (7th Edition):

Syrmou, Areti. “Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο.” 2018. Web. 29 Oct 2020.

Vancouver:

Syrmou A. Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10442/hedi/42449.

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

Council of Science Editors:

Syrmou A. Έλεγχος ασθενών με συγγενείς ανωμαλίες με τη μέθοδο του μοριακού καρυοτύπου/ Array-CGH: συσχέτιση του γονότυπου με το φαινότυπο. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. Available from: http://hdl.handle.net/10442/hedi/42449

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


Stellenbosch University

2. Steyn, Louis Johannes. Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae).

Degree: MSc, Genetics, 2016, Stellenbosch University

ENGLISH ABSTRACT: Diuraphis noxia Kurdjumov (Russian wheat aphid (RWA)), is an economically important agricultural pest that causes substantial losses in small grain production, particularly wheat… (more)

Subjects/Keywords: Russian wheat aphid  – Karyotyping; Diuraphis noxia (Hemiptera: Aphididae)  – Characterisation; Russian wheat aphid  – Molecular genetics; UCTD

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

APA (6th Edition):

Steyn, L. J. (2016). Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae). (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/100215

Chicago Manual of Style (16th Edition):

Steyn, Louis Johannes. “Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae).” 2016. Masters Thesis, Stellenbosch University. Accessed October 29, 2020. http://hdl.handle.net/10019.1/100215.

MLA Handbook (7th Edition):

Steyn, Louis Johannes. “Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae).” 2016. Web. 29 Oct 2020.

Vancouver:

Steyn LJ. Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae). [Internet] [Masters thesis]. Stellenbosch University; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10019.1/100215.

Council of Science Editors:

Steyn LJ. Karyotyping and in silico characterisation of the chromosomes of Diuraphis noxia (Hemiptera: Aphididae). [Masters Thesis]. Stellenbosch University; 2016. Available from: http://hdl.handle.net/10019.1/100215

3. Giannikou, Krinio. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Intellectual Disability (ID) is a very clinically and genetically heterogeneous neurodevelopmental entity, thus raising difficulties on genetic evaluation and diagnosis. Hitherto, only a few cases… (more)

Subjects/Keywords: Μικροσυστοιχίες συγκριτικού γενωμικού υβριδισμού; Νοητική υστέρηση; Ποικιλομορφίες αριθμού αντιγράφων; Μικροελλείμματα/Μικροδιπλασιασμοί; Μοριακός καρυότυπος; Microarray comparative genomic hybridization; Intellectual disability; Copy number variations (CNVs); Microdeletion/Microduplication; Molecular karyotyping

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APA (6th Edition):

Giannikou, K. (2014). Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42161

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):

Giannikou, Krinio. “Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 29, 2020. http://hdl.handle.net/10442/hedi/42161.

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

MLA Handbook (7th Edition):

Giannikou, Krinio. “Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH).” 2014. Web. 29 Oct 2020.

Vancouver:

Giannikou K. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10442/hedi/42161.

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

Council of Science Editors:

Giannikou K. Ανίχνευση υπομικροσκοπικών χρωμοσωμικών διαταραχών σε ασθενείς με νοητική υστέρηση αγνώστου αιτιολογίας με τη μέθοδο των μικροσυστοιχιών γενωμικού συγκριτικού υβριδισμού (array-CGH). [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/42161

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

4. Knijnenburg, Jeroen. Advanced genome-wide screening in human genomic disorders.

Degree: 2009, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

Subjects/Keywords: Genomic disorders; Mental retardation; Array-CGH; MLPA; FISH; Molecular karyotyping; Genomic disorders; Mental retardation; Array-CGH; MLPA; FISH; Molecular karyotyping

Karyotyping of human cells was developed in the 1950’s, stimulated by the publication of Tjio and… …trypsin mediated G-banding, is nowadays one of the most widely used techniques for karyotyping… …molecular cytogenetic techniques. Discovery of chromosome banding has been the most important tool… …balanced carriers were found. To facilitate karyotyping, automated systems have been developed… …images with segmentation and karyotyping of the chromosomes, after 10 Chapter 1 which the… 

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APA (6th Edition):

Knijnenburg, J. (2009). Advanced genome-wide screening in human genomic disorders. (Doctoral Dissertation). Department of Molecular Cell Biology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/13531

Chicago Manual of Style (16th Edition):

Knijnenburg, Jeroen. “Advanced genome-wide screening in human genomic disorders.” 2009. Doctoral Dissertation, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed October 29, 2020. http://hdl.handle.net/1887/13531.

MLA Handbook (7th Edition):

Knijnenburg, Jeroen. “Advanced genome-wide screening in human genomic disorders.” 2009. Web. 29 Oct 2020.

Vancouver:

Knijnenburg J. Advanced genome-wide screening in human genomic disorders. [Internet] [Doctoral dissertation]. Department of Molecular Cell Biology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2009. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1887/13531.

Council of Science Editors:

Knijnenburg J. Advanced genome-wide screening in human genomic disorders. [Doctoral Dissertation]. Department of Molecular Cell Biology, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2009. Available from: http://hdl.handle.net/1887/13531

5. Krgović, Danijela. Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra.

Degree: 2015, Univerza v Mariboru

 Kljub intenzivni genetski obravnavi otrok z razvojno–nevrološkimi motnjami pri skoraj polovici obravnavanih ostaja vzrok motnje še vedno nepojasnjen. V zadnjih dveh desetletjih je uvedba tehnologije… (more)

Subjects/Keywords: Strukturne genomske variabilnosti; molekularna kariotipizacija; duševna manjrazvitost/razvojni zaostanek; motnje avtističnega spektra; slovenska populacija; Copy number variation; molecular karyotyping; developmental delay/intellectual disabilities; autism spectrum disorders; multiple congenital anomalies; Slovenian population

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APA (6th Edition):

Krgović, D. (2015). Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra. (Doctoral Dissertation). Univerza v Mariboru. Retrieved from https://dk.um.si/IzpisGradiva.php?id=47750 ; https://dk.um.si/Dokument.php?id=71060&dn= ; https://plus.si.cobiss.net/opac7/bib/512489016 ?lang=sl

Chicago Manual of Style (16th Edition):

Krgović, Danijela. “Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra.” 2015. Doctoral Dissertation, Univerza v Mariboru. Accessed October 29, 2020. https://dk.um.si/IzpisGradiva.php?id=47750 ; https://dk.um.si/Dokument.php?id=71060&dn= ; https://plus.si.cobiss.net/opac7/bib/512489016 ?lang=sl.

MLA Handbook (7th Edition):

Krgović, Danijela. “Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra.” 2015. Web. 29 Oct 2020.

Vancouver:

Krgović D. Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra. [Internet] [Doctoral dissertation]. Univerza v Mariboru; 2015. [cited 2020 Oct 29]. Available from: https://dk.um.si/IzpisGradiva.php?id=47750 ; https://dk.um.si/Dokument.php?id=71060&dn= ; https://plus.si.cobiss.net/opac7/bib/512489016 ?lang=sl.

Council of Science Editors:

Krgović D. Analiza klinično pomembnih strukturnih genomskih variabilnosti pri slovenskih otrocih z nepojasnjenim razvojnim ali duševnim zaostankom, s prirojenimi nepravilnostmi in z motnjami avtističnega spektra. [Doctoral Dissertation]. Univerza v Mariboru; 2015. Available from: https://dk.um.si/IzpisGradiva.php?id=47750 ; https://dk.um.si/Dokument.php?id=71060&dn= ; https://plus.si.cobiss.net/opac7/bib/512489016 ?lang=sl

6. Bayani, Jane Marie. The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma.

Degree: 2013, University of Toronto

Ovarian cancer (OCa) remains the leading cause of death due to a gynecologic malignancy in North American women, and the pathogenesis of this disease is… (more)

Subjects/Keywords: Molecular Cytogenetics; Chromosomal instability; Fluorescence in situ Hybridization; Spectral Karyotyping; Comparative Genomic Hybridization; Cancer; 0571; 0307; 0380

…58 3.2.3 Spectral Karyotyping… …100 5.2.1 Fluorescence in situ Hybridization (FISH), Spectral Karyotyping (… …interfering Ribonucleic Acid SKY Spectral Karyotyping SNP Single Nucleotide Polymorphism SPORE… …differences between the molecular subtypes (reviewed by Karst and Drapkin, 2010). There… …represents distant metastasis to the chest, liver and other organs 1.5 Molecular Pathology 1.5.1… 

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APA (6th Edition):

Bayani, J. M. (2013). The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35774

Chicago Manual of Style (16th Edition):

Bayani, Jane Marie. “The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma.” 2013. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/35774.

MLA Handbook (7th Edition):

Bayani, Jane Marie. “The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma.” 2013. Web. 29 Oct 2020.

Vancouver:

Bayani JM. The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/35774.

Council of Science Editors:

Bayani JM. The Impact of Chromosomal Aberrations on the Regulation of Kallikrein 6 Expression in Serous Ovarian Carcinoma. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35774

.