(Q51325397)
Statements
Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies (English)
Marjolein H Willemsen
Nicole de Leeuw
Arjan P M de Brouwer
Rolph Pfundt
Jayne Y Hehir-Kwa
Helger G Yntema
Willy M Nillesen
Bert B A de Vries
Tjitske Kleefstra