Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation-Reference-Cited by-同舟云学术

Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation

Published:2006-11-15 Issue:22 Volume:140A Page:2416-2425
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Robin Nathaniel H.,Taylor Clare J.,McDonald-McGinn Donna M.,Zackai Elaine H.,Bingham Peter,Collins Kevin J.,Earl Dawn,Gill Deepak,Granata Tiziana,Guerrini Renzo,Katz Naomi,Kimonis Virginia,Lin Jean-Pierre,Lynch David R.,Mohammed Shehla N.,Massey Roger F.,McDonald Marie,Rogers R. Curtis,Splitt Miranda,Stevens Cathy A.,Tischkowitz Marc D.,Stoodley Neil,Leventer Richard J,Pilz Daniela T.,Dobyns William B.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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