Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
about
FOXC2 mutations in familial and sporadic spinal extradural arachnoid cyst.Genotypes and phenotypes of 162 families with a glomulin mutation.Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.Distichiasis in a ferret (Mustela putorius furo).
P2860
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年學術文章
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name
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@en
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@nl
type
label
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@en
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@nl
prefLabel
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@en
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@nl
P2093
P2860
P50
P356
P1476
Microcephaly, intellectual imp ...... etion and a Glomulin mutation.
@en
P2093
Jeffrey W Innis
Matthew G Butler
Peter Strouse
Susan L Dagenais
Thomas W Glover
P2860
P304
P356
10.1002/AJMG.A.35229
P407
P577
2012-03-09T00:00:00Z