HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
about
Cellular and Molecular Underpinnings of Neuronal Assembly in the Central Auditory System during Mouse Development.The genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2.Exome Sequence Analysis of 14 Families With High Myopia.The development of the mammalian outer and middle ear.Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia.Genome-wide association scan suggests basis for microtia in Awassi sheep.Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.
P2860
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P2860
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
description
2013 nî lūn-bûn
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2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
@wuu
name
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@ast
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@en
type
label
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@ast
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@en
prefLabel
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@ast
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@en
P2093
P2860
P356
P1433
P1476
HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.
@en
P2093
Barbara McDonough
Cecilia C Helwig
Christine E Seidman
Gabriel Osorno
Jonathan G Seidman
Kerry K Brown
Lourdes Quintanilla-Dieck
Lucas M Viana
Maria A Artunduaga
Patricia Jarrin
P2860
P304
P356
10.1002/HUMU.22367
P577
2013-07-11T00:00:00Z