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The genetic basis of Cowden's syndrome: three novel mutations in PTEN/MMAC1/TEP1.
Tsou, H C; Ping, X L; Xie, X X; Gruener, A C; Zhang, H; Nini, R; Swisshelm, K; Sybert, V; Diamond, T M; Sutphen, R; Peacocke, M.
Affiliation
  • Tsou HC; Department of Dermatology, Columbia University, College of Physicians and Surgeons, New York, NY 10032, USA.
Hum Genet ; 102(4): 467-73, 1998 Apr.
Article in En | MEDLINE | ID: mdl-9600246
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Collection: 01-internacional Database: MEDLINE Main subject: Hamartoma Syndrome, Multiple / Genes, Tumor Suppressor / Protein Tyrosine Phosphatases / Germ-Line Mutation / Phosphoric Monoester Hydrolases / Tumor Suppressor Proteins Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans Language: En Journal: Hum Genet Year: 1998 Document type: Article Affiliation country: Estados Unidos Country of publication: Alemania
Search on Google
Add to My VHL
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Hamartoma Syndrome, Multiple / Genes, Tumor Suppressor / Protein Tyrosine Phosphatases / Germ-Line Mutation / Phosphoric Monoester Hydrolases / Tumor Suppressor Proteins Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans Language: En Journal: Hum Genet Year: 1998 Document type: Article Affiliation country: Estados Unidos Country of publication: Alemania