Biallelic Gins2 Variant P.(Arg114Leu) Causes Meier-Gorlin Syndrome with Craniosynostosis

AuthID
P-015-D9E
8
Author(s)
Miller, KA
·
McQuaid, M
·
Koelling, N
·
Wilkie, AOM
·
Wurtele, H
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de Brouwer, APM
·
Tipo de Documento
Article
Year published
2021
Publicado
in Journal of Medical Genetics, ISSN: 0022-2593
Volume: 59, Número: 8, Páginas: 776-780
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Publication Identifiers
Source Identifiers
ISSN: 0022-2593
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