Griffith Andrew | Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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概要
- GRIFFITH Andrew Jの詳細を見る
- 同名の論文著者
- Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Healthの論文著者
関連著者
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Van Camp
Department Of Haematology And Immunology Free′ University Brussels′ Hokkaido University. Vol. 2.
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Park Hong-Joon
Soree Ear Clinic
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Riazuddin Sheikh
Allama Iqbal Medical College-jinnah Hospital Complex University Of Health Sciences
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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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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
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Kim Un-kyung
Department Of Biology College Of Natural Sciences Kyungpook National University
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Park Hong-joon
Soree Ear Clinics
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Kwon Tae-jun
Department Of Biology College Of Natural Sciences Kyungpook National University
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CHO Hyun-Ju
Department of Biology, College of Natural Sciences, Kyungpook National University
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BAEK Jeong-In
Department of Biology, College of Natural Sciences, Kyungpook National University
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BEN-YOSEF Tamar
Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders/National Institutes of Health (NIDCD/NIH)
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GRIFFITH Andrew
Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders/National Institutes of Health (NIDCD/NIH)
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Cho Hyun-ju
Department Of Biology College Of Natural Sciences Kyungpook National University
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Baek Jeong-in
Department Of Biology College Of Natural Sciences Kyungpook National University
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders/national Institutes Of Health (nidcd/nih)
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Griffith Andrew
Otolaryngology Branch Nidcd/nih
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Ben-yosef Tamar
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders/national Institutes Of Health (nidcd/nih)
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HILGERT Nele
Department of Medical Genetics, University of Antwerp (UA)
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MONAHAN Kelly
Otolaryngology Branch, NIDCD/NIH
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KURIMA Kiyoto
Otolaryngology Branch, NIDCD/NIH
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LI Cindy
Section on Hereditary Disorders of the Ear, House Ear Institute
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FRIEDMAN Rick
Section on Hereditary Disorders of the Ear, House Ear Institute
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ANWAR Saima
National Center of Excellence in Molecular Biology, Punjab University
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TASNEEM Saba
National Center of Excellence in Molecular Biology, Punjab University
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JALEEL Ateeq-ul
National Center of Excellence in Molecular Biology, Punjab University
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KHAN Shahid
National Center of Excellence in Molecular Biology, Punjab University
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FRIEDMAN Thomas
Laboratory of Molecular Genetics, Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health
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RIAZUDDIN Sheikh
National Center of Excellence in Molecular Biology, Punjab University
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Li Cindy
Section On Hereditary Disorders Of The Ear House Ear Institute
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Khan Shahid
National Center Of Excellence In Molecular Biology Punjab University
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Anwar Saima
National Center Of Excellence In Molecular Biology Punjab University
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Tasneem Saba
National Center Of Excellence In Molecular Biology Punjab University
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Hilgert Nele
Department Of Medical Genetics University Of Antwerp (ua)
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Monahan Kelly
Otolaryngology Branch Nidcd/nih
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Kurima Kiyoto
Otolaryngology Branch Nidcd/nih
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Friedman Rick
Section On Hereditary Disorders Of The Ear House Ear Institute
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Van Camp
Department Of Medical Genetics University Of Antwerp (ua)
著作論文
- Amino acid 572 in TMC1 : hot spot or critical functional residue for dominant mutations causing hearing impairment
- Evidence for a founder mutation causing DFNA5 hearing loss in East Asians
- SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis