Kimberling William | Department Of Genetics Boys Town National Research Hospital
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概要
- KIMBERLING William J.の詳細を見る
- 同名の論文著者
- Department Of Genetics Boys Town National Research Hospitalの論文著者
関連著者
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SHINKAWA HIDEICHI
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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Usami Shinichi
Department Of Otolaryngology Shinshu University School Of Medicine
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USAMI Shin-ichi
Department of Otorhinolaryngology, Shinshu University School of Medicine
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Usami S
Shinshu Univ. School Of Medicine Matsumoto Jpn
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Usami Shin-ichi
Department Of Otorhinolaryngology Shinshu University School Of Medicine
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Abe Satoko
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science
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ABE Satoko
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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KIMBERLING William
Department of Genetics, Boys Town National Research Hospital
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Shinkawa Hideichi
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
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Shinkawa Hideichi
Department Of Otolaryngology Hirosaki University School Of Medicine
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Kimberling William
Department Of Genetics Boys Town National Research Hospital
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NAMBA Atsushi
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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AKITA Jiro
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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DEFFENBACHER Karen
Department of Genetics, Boys Town National Research Hospital
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KUMAR Sharawan
Department of Genetics, Boys Town National Research Hospital
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Akita Jiro
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
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Namba Atsushi
Department Of Otolaryngology Hirosaki University School Of Medicine
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Namba Atsushi
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
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Kumar Sharawan
Department Of Genetics Boys Town National Research Hospital
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Deffenbacher Karen
Department Of Genetics Boys Town National Research Hospital
著作論文
- Genetic features of hearing loss associated with ear anomalies : PDS and EYA1 mutation analysis
- Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a gene responsible in Japanese
- EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family