Molecular and clinical studies of X-linked deafness among Pakistani families
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概要
- 論文の詳細を見る
- 2011-07-01
著者
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Khan Shaheen
National Center Of Excellence In Molecular Biology University Of The Punjab
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Riazuddin Sheikh
Allama Iqbal Medical College-jinnah Hospital Complex University Of Health Sciences
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WARYAH Ali
National Center of Excellence in Molecular Biology, University of the Punjab
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AHMED Zubair
Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head and Neck Surgery, Cincinnati Children Hospital Research Foundation
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BHINDER Munir
National Center of Excellence in Molecular Biology, University of the Punjab
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CHOO Daniel
Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head and Neck Surgery, Cincinnati Children Hospital Research Foundation
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SISK Robert
Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Research Foundation
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SHAHZAD Mohsin
National Center of Excellence in Molecular Biology, University of the Punjab
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FRIEDMAN Thomas
Section on Human Genetics, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health
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RIAZUDDIN Saima
Laboratory of Molecular Genetics, Division of Pediatric Otolaryngology Head and Neck Surgery, Cincinnati Children Hospital Research Foundation
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Waryah Ali
National Center Of Excellence In Molecular Biology University Of The Punjab
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Sisk Robert
Division Of Pediatric Ophthalmology Cincinnati Children's Hospital Research Foundation
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Choo Daniel
Laboratory Of Molecular Genetics Division Of Pediatric Otolaryngology Head And Neck Surgery Cincinnati Children Hospital Research Foundation
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Bhinder Munir
National Center Of Excellence In Molecular Biology University Of The Punjab
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Shahzad Mohsin
National Center Of Excellence In Molecular Biology University Of The Punjab
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Riazuddin Saima
Laboratory Of Molecular Genetics Division Of Pediatric Otolaryngology Head And Neck Surgery Cincinnati Children Hospital Research Foundation
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Friedman Thomas
Section On Human Genetics Laboratory Of Molecular Genetics National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Ahmed Zubair
Laboratory Of Molecular Genetics Division Of Pediatric Otolaryngology Head And Neck Surgery Cincinnati Children Hospital Research Foundation
関連論文
- Molecular and clinical studies of X-linked deafness among Pakistani families
- SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis
- USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1
- Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population