Portuguese Case of Smith-Mccort Syndrome Caused by a New Mutation in the Dymeclin (Flj20071) Gene

AuthID
 P-003-PE1
4
Author(s)
Fernandes, HC
·
Almelda, MR
Tipo de Documento
Article
Year published
2009
Publicado
in CLINICAL DYSMORPHOLOGY, ISSN: 0962-8827
Volume: 18, Número: 1, Páginas: 41-44 (4)
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Pubmed®
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Publication Identifiers
Pubmed: 19005420
SCOPUS: 2-s2.0-58149215979
Wos: WOS:000262213100008
Source Identifiers
ISSN: 0962-8827
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