Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies-Reference-Cited by-同舟云学术

Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies

Published:2012-11 Issue:11 Volume:55 Page:586-598
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Willemsen Marjolein H.,de Leeuw Nicole,de Brouwer Arjan P.M.,Pfundt Rolph,Hehir-Kwa Jayne Y.,Yntema Helger G.,Nillesen Willy M.,de Vries Bert B.A.,van Bokhoven Hans,Kleefstra Tjitske

Funder

Consortium VG Oost-Nederland

The Netherlands Organization for Health Research and Development

GENCODYS

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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