Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes*-Reference-Cited by-同舟云学术

Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes*

Published:2001-10 Issue:4 Volume:69 Page:704-711
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Zhou Xiao-Ping,Woodford-Richens Kelly,Lehtonen Rainer,Kurose Keisuke,Aldred Micheala,Hampel Heather,Launonen Virpi,Virta Sanno,Pilarski Robert,Salovaara Reijo,Bodmer Walter F.,Conrad Beth A.,Dunlop Malcolm,Hodgson Shirley V.,Iwama Takeo,Järvinen Heikki,Kellokumpu Ilmo,Kim J.C.,Leggett Barbara,Markie David,Mecklin Jukka-Pekka,Neale Kay,Phillips Robin,Piris Juan,Rozen Paul,Houlston Richard S.,Aaltonen Lauri A.,Tomlinson Ian P.M.,Eng Charis

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference35 articles.

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3. Absence of germline mutations in MINPP1, a phosphatase-encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations;Dahia;J Med Genet,2000

4. Will the real Cowden syndrome please stand up: revised diagnostic criteria;Eng;J Med Genet,2000

5. To be or not to BMP;Eng;Nat Genet,2001

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