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Biallelic Gins2 Variant P.(Arg114Leu) Causes Meier-Gorlin Syndrome with Craniosynostosis
AuthID
P-016-B1Y
8
Author(s)
Sá M.J.N.
·
Miller K.A.
·
McQuaid M.
·
Koelling N.
·
Wilkie A.O.M.
·
Wurtele H.
·
De Brouwer A.P.M.
·
Oliveira J.
Document Type
Article
Year published
2022
Published
in
Journal of Medical Genetics,
ISSN: 00222593
Volume: 59, Issue: 8, Pages: 776-780 (4)
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Scopus
®
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®
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®
Metadata
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Publication Identifiers
DOI
:
10.1136/jmedgenet-2020-107572
Pubmed
: 34353863
SCOPUS
: 2-s2.0-85112319638
Source Identifiers
ISSN
: 00222593
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