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

AuthID
P-00A-87Z

Author(s)

Vissers, LELM

Bonetti, M

Overman, JP

Nillesen, WM

Frints, SGM

de Ligt, J

Zampino, G

Justino, A

Machado, JC

Schepens, M

Brunner, HG

Veltman, JA

Scheffer, H

Gros, P

Costa, JL

Tartaglia, M

van der Burgt, I

Yntema, HG

den Hertog, J

Document Type

Article

Year published

2015

Published

in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813

Volume: 23, Issue: 3, Pages: 317-324 (8)

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Scopus^®

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Pubmed^®

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Publication Identifiers

DOI: 10.1038/ejhg.2014.115

Pubmed: 24939586

SCOPUS: 2-s2.0-84938421325

Wos: WOS:000349670900007

Source Identifiers

ISSN: 1018-4813

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

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

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