Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identifiedGLI3 mutations-Reference-Cited by-同舟云学术

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Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identifiedGLI3 mutations

Published:2003-06-03 Issue:1 Volume:120A Page:49-58
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Debeer Philippe,Peeters H.,Driess S.,De Smet L.,Freese K.,Matthijs G.,Bornholdt D.,Devriendt K.,Grzeschik K.-H.,Fryns J.-P.,Kalff-Suske M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference26 articles.

1. Greig cephalopolysyndactyly syndrome in a large family

2. Greig cephalopolysyndactyly: report of 13 affected individuals in three families

3. The greig cephalopolysyndactyly syndrome in a canadian family

4. Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13)

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