Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher.
about
A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3)A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.Gene regulation in the magnocellular hypothalamo-neurohypophysial system.Spectrum of Third Window Abnormalities: Semicircular Canal Dehiscence and Beyond.Frequency and specific characteristics of the incomplete partition type III anomaly in children.Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA.Molecular characterization of a novel X-linked syndrome involving developmental delay and deafness.A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families
P2860
Q28285821-2E9D46D6-4047-4AEA-B0CA-E99D9CE1B67BQ30363026-A1E9D25A-A0A5-410C-828F-266B4298B128Q30367238-87E09551-4A37-4BDD-A1E3-97263FB07B7DQ30398827-A2C2CC8B-B767-4824-8202-D1E4C8B723DBQ30411037-52D6FDA1-C849-4A83-8ED6-0405A18C36A1Q33953261-749459D4-10A7-4952-94DD-4369F0A59543Q38937301-61B6DA31-DEAE-46AF-BB05-3ABDCBC1B740Q50422794-8C4CC0F8-38FD-4E50-A5F4-C8910BA5A899Q50435313-9705DC4A-51CE-4C46-8EC6-F39FE9AB299EQ50438244-BC26FE94-30FC-4EFC-9453-DBC59854399EQ51975164-E8016F21-F976-49E9-AAE1-BA0233C5DE87Q55221358-A18044D5-9F10-4844-B562-4DBFCF70CC9CQ58765599-58CED925-4641-41CC-859E-A24FF1E1B8AA
P2860
Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@en
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@nl
type
label
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@en
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@nl
prefLabel
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@en
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@nl
P2093
P2860
P1476
Molecular analysis of the POU3 ...... ess with perilymphatic gusher.
@en
P2093
D F Wilson
J M Talbot
L S Parnes
N Fischel-Ghodsian
R A Friedman
Y Bykhovskaya
P2860
P304
P356
10.1177/000348949710600411
P577
1997-04-01T00:00:00Z