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
Document Type
Article
Year published
2009
Published
in CLINICAL DYSMORPHOLOGY, ISSN: 0962-8827
Volume: 18, Issue: 1, Pages: 41-44 (4)
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Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 19005420
Scopus: 2-s2.0-58149215979
Wos: WOS:000262213100008
Source Identifiers
ISSN: 0962-8827
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