A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24
about
A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlationAudiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA.A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p
P2860
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@ast
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@en
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@nl
type
label
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@ast
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@en
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@nl
prefLabel
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@ast
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@en
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@nl
P2093
P2860
P1476
A gene for autosomal dominant ...... 2) maps to chromosome 11q22-24
@en
P2093
Balemans W
Govaerts PJ
Offeciers FE
Schatteman I
Van Camp G
Van Laer L
Van de Heyning PH
P2860
P304
P407
P577
1997-05-01T00:00:00Z