Naruse I. | Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chiba
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- 同名の論文著者
- Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chibaの論文著者
関連著者
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Naruse I.
Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chiba
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Keino H.
Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chiba
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Naruse I.
Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chiba Children's Hospital:institute For Developmental Research Aichi Human Service Center
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Keino H.
Institute For Developmental Research Aichi Human Service Center
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NARUSE I.
Institute for Developmental Research, Aichi Prefectural Colony and Department of Anatomy, Hiroshim a
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TANIGUCHI M.
Institute for Developmental Research, Aichi Human Service Center
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Naruse I.
Institute For Developmental Research Aichi Human Service Center
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Taniguchi M.
Institute For Developmental Research Aichi Human Service Center
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NARUSE I.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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YAMADA Y.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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Ishikiriyama S.
Congenital Anomaly Research Center Faculty Of Medicine Kyoto University:department Of Genetics Chiba
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KEINO H.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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Yamada Y.
Institut fur Theoretische Physik, Universitdt Wien
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HUI C.-C.
Institute for Developmental Research, Aichi Human Service Center
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Hui C.-c.
Institute For Developmental Research Aichi Human Service Center:the Hospital For Sick Children
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Naruse I.
School of Health Science, Faculty of Medicine, Tottori University
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Naruse I.
School Of Health Science Faculty Of Medicine Tottori University
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TANAKA Y.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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MAEKAWA T.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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ISHII S.
Congenital Anomaly Research Center, Faculty of Medicine, Kyoto University
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Shiota K.
Congenital Anomaly Research Center:department Of Anatomy And Developmental Biology Kyoto University Faculty Of Medicine:aichi Human Service Center
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Shiota K.
Congenital Anomaly Research Center Faculty Of Medicine Kyoto University And Merrell Dow Research Institute Merrell Dow Pharmaceuticals Co.. Ltd.
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HIROSE M.
Congenital Anomaly Research Center
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NARUSE I.
Congenital Anomaly Research Center:Department of Anatomy and Developmental Biology, Kyoto University Faculty of Medicine:Aichi Human Service Center
著作論文
- P-52 DNA Isolation from the Human Embryos Fixed 30 Years Ago and Sex Determination Using PCR Method.
- Pdn/Pdn (Genetic Polydactyly / Arhinencephaly) Mouse Is a Homologue of Greig Cephalopolysyndactyly Syndrome : Poster Session
- Genetic Polydactyly/Arhinencephaly Mouse (Pdn/Pdn) is a Homologous Animal of Human Greig Cephalopolysyndactyly Syndrome (Gcps) : Paper Presented from Platform
- Phenotypic differences In the brains and limbs of mutant mice caused by differences of Gli3 gene expression levels : Papers Presented from Platform
- Fetal laser surgery exo utero in mice : III. FETAL SURGERY : BASIC AND CLINICAL ASPECTS : Symposia
- Gli3 gene expression during mouse limb morphogenesis : The 35th Annual Meeting of the Japanese Teratology Society
- Non-attachment of the olfactory nerve fibers to the telencephalon in genetic arhinencephalic mouse embryos, Pdn/Pdn : The 35th Annual Meeting of the Japanese Teratology Society
- Decrease of Gli3 gene transcription in genetic polydactylic and arhinencephalic mouse (Pdn/Pdn ) : Abstracts of Papers Presented at the Thirty-Fourth Annual Meeting of the Japanese Teratology Society Kochi, Japan July14-16, 1994
- The role of apoptosis in the manifestation of polydactyly and arhinencephaly in genetic mutant mouse, Pdn/Pdn : Abstracts of Papers Presented at the Thirty-Fourth Annual Meeting of the Japanese Teratology Society Kochi, Japan July14-16, 1994
- B-09 Phenotypic Similarity in Rubinstein-Taybi Syndrome and Knockout Mice in Cbp Gene.
- MS-4 Greig Cephalopolysyndactyly Syndrome (GCPS) and its Mouse Homolog, Pdn/Pdn.(HUMAN CONGENITAL ANOMALIES AND ANIMAL MODELS)