A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects-Reference-Cited by-同舟云学术

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A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects

Published:2002-04-10 Issue:5 Volume:110 Page:422-428
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

de la Cruz June M.,Bamford Richard N.,Burdine Rebecca D.,Roessler Erich,Barkovich James A.,Donnai Dian,Schier Alexander F.,Muenke Maximilian

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0709-3.pdf

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