X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4
about
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing loss.Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.Human inversions and their functional consequencesEstrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay.Frequency and specific characteristics of the incomplete partition type III anomaly in children.
P2860
X-linked deafness-2 (DFNX2) phenotype associated with a paracentric inversion upstream of POU3F4
description
2014 nî lūn-bûn
@nan
2014 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մարտին 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
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@ast
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@en
type
label
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@ast
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@en
prefLabel
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@ast
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@en
P2093
P2860
P356
P1476
X-linked deafness-2 (DFNX2) ph ...... c inversion upstream of POU3F4
@en
P2093
Cynthia C Morton
Gregory J Anger
Jennifer J MacKenzie
Karen Harrison
Kerry K Brown
Kyle McKenzie
Susan Crocker
P2860
P356
10.1044/1059-0889(2013/13-0018)
P577
2014-03-01T00:00:00Z