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

AuthID
P-00V-SVP
8
Author(s)
Miller, KA
·
McQuaid, M
·
Koelling, N
·
Wilkie, AOM
·
Wurtele, H
·
De Brouwer, APM
·
Oliveira, J
Document Type
Article in Press
Year published
2021
Published
in JOURNAL OF MEDICAL GENETICS, ISSN: 0022-2593
Indexing
Publication Identifiers
Wos: WOS:000725043200001
Source Identifiers
ISSN: 0022-2593
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