Haploinsufficiency of the HOXA Gene Cluster, in a Patient with Hand-Foot-Genital Syndrome, Velopharyngeal Insufficiency, and Persistent Patent Ductus Botalli-Reference-Cited by-同舟云学术

Haploinsufficiency of the HOXA Gene Cluster, in a Patient with Hand-Foot-Genital Syndrome, Velopharyngeal Insufficiency, and Persistent Patent Ductus Botalli

Published:1999-07 Issue:1 Volume:65 Page:249-251
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Devriendt Koenraad,Jaeken Jaak,Matthijs Gert,Van Esch Hilde,Debeer Philippe,Gewillig Marc,Fryns Jean-Pierre

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5;Chisaka;Nature,1991

2. Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome;Devriendt;J Med Genet,1997

3. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract;Goodman;Proc Natl Acad Sci USA,1997

4. Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families;Goodman;Am J Hum Genet,1998

5. Novel HOXA-13 mutations and phenotypic spectrum of hand-foot-genital syndrome;Goodman;Am J Hum Genet Suppl,1998

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