Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome-Reference-Cited by-同舟云学术

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

Published:1997-05 Issue:1 Volume:16 Page:64-67
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Liaw Danny,Marsh Debbie J.,Li Jing,Dahia Patricia L. M.,Wang Steven I.,Zheng Zimu,Bose Shikha,Call Katherine M.,Tsou Hui C.,Peacoke Monica,Eng Charis,Parsons Ramon

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0597-64.pdf

Reference16 articles.

1. Lloyd, K.M. & Dennis, M. Cowden's disease: a possible new symptom complex with multiple system involvement. Ann. Intern. Medi. 58, 136–142 (1963).

2. Mallory, S.B. Cowden syndrome (multiple hamartoma symdrome). Derm. Clinics. 13, 27–31 (1995).

3. Longy, M. & Lacomb, D. Cowden disease. Report of a family and review. Ann. Genet. 39, 35–42 (1996).

4. Padberg, G.W., Schot, J.D.L., Vielvoye, G.J., Bots, G.T.A.M. & & deBeer, F.C. Lhermitte-Duclos disease and Cowden syndrom: a single phakomatosis. Ann. Neurol. 29, 517–523 (1991).

5. Nelen, M.R. et al. Localization of the gene for Cowden disease to chromosome 10q22–23. Nature Genet. 13, 114–116 (1996).

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