KIMBERLING William | Department of Genetics, Boys Town National Research Hospital
スポンサーリンク
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
-
SHINKAWA HIDEICHI
Department of Otorhinolaryngology, Hirosaki University School of Medicine
-
Usami Shinichi
Department Of Otolaryngology Shinshu University School Of Medicine
-
USAMI Shin-ichi
Department of Otorhinolaryngology, Shinshu University School of Medicine
-
Usami S
Shinshu Univ. School Of Medicine Matsumoto Jpn
-
Usami Shin-ichi
Department Of Otorhinolaryngology Shinshu University School Of Medicine
-
Abe Satoko
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science
-
ABE Satoko
Department of Otorhinolaryngology, Hirosaki University School of Medicine
-
KIMBERLING William
Department of Genetics, Boys Town National Research Hospital
-
Shinkawa Hideichi
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
-
Shinkawa Hideichi
Department Of Otolaryngology Hirosaki University School Of Medicine
-
Kimberling William
Department Of Genetics Boys Town National Research Hospital
-
NAMBA Atsushi
Department of Otorhinolaryngology, Hirosaki University School of Medicine
-
AKITA Jiro
Department of Otorhinolaryngology, Hirosaki University School of Medicine
-
DEFFENBACHER Karen
Department of Genetics, Boys Town National Research Hospital
-
KUMAR Sharawan
Department of Genetics, Boys Town National Research Hospital
-
Akita Jiro
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
-
Namba Atsushi
Department Of Otolaryngology Hirosaki University School Of Medicine
-
Namba Atsushi
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
-
Kumar Sharawan
Department Of Genetics Boys Town National Research Hospital
-
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