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

AuthID
 P-006-7XH
18
Author(s)
Pinto, C
·
Peixoto, A
·
Veiga, I
·
Mesquita, B
·
Sousa, O
·
Fragoso, M
·
Baptista, M
·
Marinho, C
·
Mangold, E
·
Vaccaro, C
·
Evans, DG
·
Farrington, S
·
Dunlop, MG
·
Document Type
Article
Year published
2013
Published
in CLINICAL GENETICS, ISSN: 0009-9163
Volume: 84, Issue: 3, Pages: 244-250 (7)
Indexing
Wos®
Scopus®
Crossref®13
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 23170986
SCOPUS: 2-s2.0-84881610774
Wos: WOS:000322979600010
Source Identifiers
ISSN: 0009-9163
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