CHINEN Yasutsugu | Department of Paediatrics, University of the Ryukyus Graduate School of Medicine
スポンサーリンク
概要
関連著者
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CHINEN Yasutsugu
Department of Paediatrics, University of the Ryukyus Graduate School of Medicine
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NARITOMI Kenji
Department of Medical Genetics, University of the Ryukyus Graduate School of Medicine
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Naritomi K
Univ. Ryukyus School Of Medicine Okinawa Jpn
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Chinen Yasutsugu
Department Of Paediatrics University Of The Ryukyus Graduate School Of Medicine
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Naritomi Kenji
Department Of Medical Genetics University Of The Ryukyus Faculty Of Medicine
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TOHMA Takaya
Department of Pediatrics, University of the Ryukyus School of Medicine
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KANAME Tadashi
Department of Biochemistry, Nagoya University School of Medicine
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Yanagi Kumiko
Department of Pathology, Tokushima University School of Dentistry
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IZUMIKAWA Yoshinori
Department of Pediatrics, University of the Ryukyus School of Medicine
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Yanagi Kumiko
Department Of Chemistry Faculty Of Science And Technology Sophia University
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Kaname Tadashi
Department Of Medical Genetics University Of The Ryukyus Graduate School Of Medicine
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HIRAYAMA Kiyotake
Department of Pediatrics, University of the Ryukyus School of Medicine
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IHA Tetsu
Department of Pediatrics, University of the Ryukyus School of Medicine
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GOYA Yoshinobu
Department of Pediatrics, University of the Ryukyus School of Medicine
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Hirayama Kiyotake
Department Of Pediatrics School Of Medicine University Of The Ryukyus
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Iha Tetsu
Department Of Pediatrics University Of The Ryukyus School Of Medicine
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Goya Yoshinobu
Department Of Pediatrics University Of The Ryukyus School Of Medicine
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Yanagi Kumiko
Department Of Medical Genetics University Of The Ryukyus Graduate School Of Medicine
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Kamei Tsutomu
Department Of Medical Genetics University Of The Ryukyus Graduate School Of Medicine
著作論文
- Novel alternative splicing of human faciogenital dysplasia 1 gene
- CHARACTERIZATION OF MARKER CHROMOSOMES BY FISH USING MICRODISSECTED PROBES FROM OLD CARNOY-FIXED CELLS : REPORT OF TWO CASES
- MEGALOCORNEA-MENTAL RETARDATION SYNDROME : AN ADDITIONAL CASE REPORT
- SMALL INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 2 (2q24.3) : FURTHER DELINEATION OF 2q MEDIAL MONOSOMY SYNDROME
- Novel alternative splicing of human faciogenital dysplasia 1 gene