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