A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.
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A mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.
description
2014 nî lūn-bûn
@nan
2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A mouse splice-site mutant and ...... al and pharyngeal development.
@ast
A mouse splice-site mutant and ...... al and pharyngeal development.
@en
A mouse splice-site mutant and ...... al and pharyngeal development.
@nl
type
label
A mouse splice-site mutant and ...... al and pharyngeal development.
@ast
A mouse splice-site mutant and ...... al and pharyngeal development.
@en
A mouse splice-site mutant and ...... al and pharyngeal development.
@nl
prefLabel
A mouse splice-site mutant and ...... al and pharyngeal development.
@ast
A mouse splice-site mutant and ...... al and pharyngeal development.
@en
A mouse splice-site mutant and ...... al and pharyngeal development.
@nl
P2093
P2860
P50
P356
P1476
A mouse splice-site mutant and ...... ial and pharyngeal development
@en
P2093
Andrew A Heggie
Georgina Caruana
Megan F Welfare
Peter G Farlie
Ravi Savarirayan
Trent Burgess
Zornitza Stark
P2860
P304
P356
10.1159/000368865
P577
2014-11-08T00:00:00Z