The Rapp–Hodgkin syndrome results from mutations of the TP63 gene-Reference-Cited by-同舟云学术

The Rapp–Hodgkin syndrome results from mutations of the TP63 gene

Published:2003-08-26 Issue:9 Volume:11 Page:700-704
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Bougeard Gaëlle,Hadj-Rabia Smaïl,Faivre Laurence,Sarafan-Vasseur Nasrin,Frébourg Thierry

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201004.pdf

Reference20 articles.

1. Rapp RS, Hodgkin WE : Anhydrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies. J Med Genet 1968; 5: 269–272.

2. Silengo MC, Davi GF, Bianco R et al: Distinctive hair changes (pili torti) in Rapp–Hodgkin ectodermal dysplasia syndrome. Clin Genet 1982; 21: 297–300.

3. Schroeder Jr HW, Sybert VP : Rapp–Hodgkin ectodermal dysplasia. J Pediat 1987; 110: 72–75.

4. Salinas CF, Montes-G GM : Rapp–Hodgkin syndrome: observations on ten cases and characteristic hair changes (pili canaliculi). Birth Defects Orig Art Ser 1988; 24: 149–168.

5. Rodini ES, Freitas JA, Richieri-Costa A : Rapp–Hodgkin syndrome: report of a Brazilian family. Am J Med Genet 1990; 36: 463–466.

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