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The Msh2 C.388_389Del Mutation Shows a Founder Effect in Portuguese Lynch Syndrome Families

AuthID
P-006-7XH

Author(s)

Pinheiro, M

Pinto, C

Peixoto, A

Veiga, I

Mesquita, B

Henrique, R

Lopes, P

Sousa, O

Fragoso, M

Dias, LM

Baptista, M

Marinho, C

Mangold, E

Vaccaro, C

Evans, DG

Farrington, S

Dunlop, MG

Teixeira, MR

Tipo de Documento

Article

Year published

2013

Publicado

in CLINICAL GENETICS, ISSN: 0009-9163

Volume: 84, Número: 3, Páginas: 244-250 (7)

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Metadata
Fontes

Publication Identifiers

DOI: 10.1111/cge.12062

Pubmed: 23170986

SCOPUS: 2-s2.0-84881610774

Wos: WOS:000322979600010

Source Identifiers

ISSN: 0009-9163

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The Msh2 C.388_389Del Mutation Shows a Founder Effect in Portuguese Lynch Syndrome Families

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The Msh2 C.388_389Del Mutation Shows a Founder Effect in Portuguese Lynch Syndrome Families

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