Refinement of the critical region of 1q41q42 microdeletion syndrome identifiesFBXO28as a candidate causative gene for intellectual disability and seizures-Reference-Cited by-同舟云学术

Refinement of the critical region of 1q41q42 microdeletion syndrome identifiesFBXO28as a candidate causative gene for intellectual disability and seizures

Published:2013-12-19 Issue:2 Volume:164 Page:441-448
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Au P.Y. Billie¹,Argiropoulos Bob¹²,Parboosingh Jillian S.¹²,Micheil Innes A.¹²

Affiliation:

1. Department of Medical Genetics; University of Calgary; Calgary Alberta Canada

2. Alberta Children's Hospital Research Institute for Child and Maternal Health; University of Calgary; Calgary Alberta Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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