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Apc or Mutyh Mutations Account for the Majority of Clinically Well-Characterized Families with Fap and Afap Phenotype and Patients with More than 30 Adenomas

AuthID
P-003-FZC

Author(s)

Filipe, B

Baltazar, C

Albuquerque, C

Fragoso, S

Lage, P

Vitoriano, I

de Ferro, SM

Claro, I

Rodrigues, P

Fidalgo, P

Chaves, P

Cravo, M

Leitao, CN

Document Type

Article

Year published

2009

Published

in CLINICAL GENETICS, ISSN: 0009-9163

Volume: 76, Issue: 3, Pages: 242-255 (14)

Indexing

Wos^®

Scopus^®

Crossref^®30

Pubmed^®

Google Scholar^®

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Sources

Publication Identifiers

DOI: 10.1111/j.1399-0004.2009.01241.x

Pubmed: 19793053

Scopus: 2-s2.0-70350137074

Wos: WOS:000270175600004

Source Identifiers

ISSN: 0009-9163

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Apc or Mutyh Mutations Account for the Majority of Clinically Well-Characterized Families with Fap and Afap Phenotype and Patients with More than 30 Adenomas

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Apc or Mutyh Mutations Account for the Majority of Clinically Well-Characterized Families with Fap and Afap Phenotype and Patients with More than 30 Adenomas

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