Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases-Reference-Cited by-同舟云学术

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases

Published:1998-11-01 Issue:12 Volume:7 Page:1907-1912
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Houlston R.,Bevan S.,Williams A.,Young J.,Dunlop M.,Rozen P.,Eng C.,Markie D.,Woodford-Richens K.,Rodriguez-Bigas M. A.,Leggett B.,Neale K.,Phillips R.,Sheridan E.,Hodgson S.,Iwama T.,Eccles D.,Bodmer W.,Tomlinson I.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/7/12/1907/1558909/7-12-1907.pdf

Reference26 articles.

1. Molecular Classification of the Inherited Hamartoma Polyposis Syndromes: Clearing the Muddied Waters

2. Association between meningioma and Cowden's disease

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