Familial CHARGE syndrome and theCHD7 gene: A recurrent missense mutation, intrafamilial recurrence and variability-Reference-Cited by-同舟云学术

Familial CHARGE syndrome and theCHD7 gene: A recurrent missense mutation, intrafamilial recurrence and variability

Published:2007 Issue:1 Volume:146A Page:43-50
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jongmans Marjolijn C.J.,Hoefsloot Lies H.,van der Donk Kim P.,Admiraal Ronald J.,Magee Alex,van de Laar Ingrid,Hendriks Yvonne,Verheij Joke B.G.M.,Walpole Ian,Brunner Han G.,van Ravenswaaij Conny M.A.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. CHARGE association looking at the future - the voice of a family support group

2. CHARGE Association: An Update and Review for the Primary Pediatrician

3. Olfactory Evaluation in Children: Application to the CHARGE Syndrome

4. Ocular Findings in CHARGE Syndrome

5. Antenatal ultrasonographic findings in the CHARGE association.

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