Molecular and clinical studies of X-linked deafness among Pakistani families.
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A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.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
Molecular and clinical studies of X-linked deafness among Pakistani families.
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2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Molecular and clinical studies of X-linked deafness among Pakistani families.
@ast
Molecular and clinical studies of X-linked deafness among Pakistani families.
@en
type
label
Molecular and clinical studies of X-linked deafness among Pakistani families.
@ast
Molecular and clinical studies of X-linked deafness among Pakistani families.
@en
prefLabel
Molecular and clinical studies of X-linked deafness among Pakistani families.
@ast
Molecular and clinical studies of X-linked deafness among Pakistani families.
@en
P2093
P2860
P356
P1476
Molecular and clinical studies of X-linked deafness among Pakistani families.
@en
P2093
Ali M Waryah
Daniel I Choo
Mohsin Shahzad
Munir A Bhinder
Robert A Sisk
Saima Riazuddin
Shaheen N Khan
Sheikh Riazuddin
Thomas B Friedman
Zubair M Ahmed
P2860
P2888
P304
P356
10.1038/JHG.2011.55
P577
2011-06-02T00:00:00Z
P5875
P6179
1028069470