Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?-Reference-Cited by-同舟云学术

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?

Published:2013-01 Issue:1 Volume:83 Page:53-65
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Shoukier M,Klein N,Auber B,Wickert J,Schröder J,Zoll B,Burfeind P,Bartels I,Alsat EA,Lingen M,Grzmil P,Schulze S,Keyser J,Weise D,Borchers M,Hobbiebrunken E,Röbl M,Gärtner J,Brockmann K,Zirn B

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01850.x/fullpdf

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4. A copy number variation morbidity map of developmental delay;Cooper;Nat Genet,2011

5. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities;Kaminsky;Genet Med,2011

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