Challenges for CNV interpretation in clinical molecular karyotyping: Lessons learned from a 1001 sample experience-Reference-Cited by-同舟云学术

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Challenges for CNV interpretation in clinical molecular karyotyping: Lessons learned from a 1001 sample experience

Published:2009-11 Issue:6 Volume:52 Page:398-403
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Buysse Karen,Delle Chiaie Barbara,Van Coster Rudy,Loeys Bart,De Paepe Anne,Mortier Geert,Speleman Frank,Menten Björn

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference37 articles.

1. Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances;Solinas-Toldo;Genes Chromosomes Cancer,1997

2. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays;Pinkel;Nat. Genet.,1998

3. Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities;Vissers;Am. J. Hum. Genet.,2003

4. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features;Shaw-Smith;J. Med. Genet.,2004

5. Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis;Vermeesch;J. Histochem. Cytochem.,2005

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