Heterozygous Germline Mutations in A2Ml1 Are Associated with a Disorder Clinically Related to Noonan Syndrome

AuthID
 P-00A-87Z
19
Author(s)
Bonetti, M
·
Overman, JP
·
de Ligt, J
·
Zampino, G
·
Schepens, M
·
Veltman, JA
·
Scheffer, H
·
Gros, P
·
Tartaglia, M
·
van der Burgt, I
·
Yntema, HG
·
den Hertog, J
Tipo de Documento
Article
Year published
2015
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 23, Número: 3, Páginas: 317-324 (8)
Indexing
Wos®
Scopus®
Crossref®43
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 24939586
SCOPUS: 2-s2.0-84938421325
Wos: WOS:000349670900007
Source Identifiers
ISSN: 1018-4813
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