A Nonsense Mutation in MSX1 Causes Witkop Syndrome-Reference-Cited by-同舟云学术

A Nonsense Mutation in MSX1 Causes Witkop Syndrome

Published:2001-07 Issue:1 Volume:69 Page:67-74
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Jumlongras Dolrudee,Bei Marianna,Stimson Jean M.,Wang Wen-Fang,DePalma Steven R.,Seidman Christine E.,Felbor Ute,Maas Richard,Seidman Jonathan G.,Olsen Bjorn R.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development;Bei;Development,1998

2. Hidrotic ectodermal dysplasia of hair, teeth, and nails: case reports and review;Chitty;J Med Genet,1996

3. The “tooth and nail” type of autosomal dominant ectodermal dysplasia;Giansanti;Oral Surg Oral Med Oral Pathol,1974

4. Dual roles of wnt signaling during chondrogenesis in the chicken limb;Hartmann;Development,2000

5. Structure and sequence of the human homeobox gene HOX7;Hewitt;Genomics,1991

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