Associated Papers
A Prospective Study of Genetic Variants in Infants with Congenital Unilateral Sensorineural Hearing Loss.
Johansson M et al.
Journal of Clinical Medicine, 2023
36675424 (PubMed )
Supplement: jcm-12-00495-s001.zip › Tables_S1_and_S2.pdf
Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
Wang R et al.
Genetic Testing and Molecular Biomarkers, 2017
The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.
Yan D et al.
Genetic Testing and Molecular Biomarkers, 2015
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
Anwar S et al.
Journal of Human Genetics, 2009
[Genetic counseling and intervention for families with deaf-mute patients based on genetic testing: analysis of 5 families].
Dai P et al.
Zhonghua Yi Xue Za Zhi, 2007
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