EYA1 gene nonsense mutation in a Japanese family with branchio-oto-renal syndrome
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-10-01
著者
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Shinomiya Noriaki
Second Department Of Pediatrics Toho University School Of Medicine
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Shinomiya Noriaki
Second Department Of Pediatrics Ohashi Hospital Toho University School Of Medicine
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UNO TAKU
Second Department of Pediatrics, Toho University School of Medicine
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SAWADA MASAKO
Second Department of Pediatrics, Toho University School of Medicine
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KUROTAKI TOSHIAKI
Second Department of Otolaringology, Toho University School of Medicine
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Sawada Masako
Second Department Of Pediatrics Toho University School Of Medicine
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Kurotaki Toshiaki
Second Department Of Otolaringology Toho University School Of Medicine
関連論文
- Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
- Wolff-Parkinson-White(WPW) Syndrome in Isolated Noncompaction of the Ventricular Myocardium(INVM) : Three Cases
- EYA1 gene nonsense mutation in a Japanese family with branchio-oto-renal syndrome
- Common acute lymphoblastic leukemia preceded by hypercalcemia in an infant