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Exome Sequencing Identifies Inppl1 Mutations as a Cause of Opsismodysplasia
AuthID
P-002-19M
16
Author(s)
Huber, C
·
Faqeih, EA
·
Bartholdi, D
·
Bole Feysot, C
·
Borochowitz, Z
·
Cavalcanti, DP
·
Frigo, A
·
Nitschke, P
·
Roume, J
·
Santos, HG
·
Shalev, SA
·
Superti Furga, A
·
Delezoide, AL
·
Le Merrer, M
·
Munnich, A
·
Cormier Daire, V
Document Type
Article
Year published
2013
Published
in
AMERICAN JOURNAL OF HUMAN GENETICS,
ISSN: 0002-9297
Volume: 92, Issue: 1, Pages: 144-149 (6)
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®
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®
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Metadata
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Publication Identifiers
DOI
:
10.1016/j.ajhg.2012.11.015
Pubmed
: 23273569
Scopus
: 2-s2.0-84872303242
Wos
: WOS:000313759000016
Source Identifiers
ISSN
: 0002-9297
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