Search Results1-13 of  13

  • KAWAME Hiroshi ID: 9000000395910

    Articles in CiNii:45

    • Clinical Spectrum and Management of Holoprosencephaly (2000)
    • 真性半陰陽を有するSRY negative XX male の1例 - 内性器の検討と成因の考察 - (1997)
    • Prader-Willi症候群とAngelman症候群 (1996)
  • KAWAME Hiroshi ID: 9000000395910

    Articles in CiNii:45

    • Clinical Spectrum and Management of Holoprosencephaly (2000)
    • 真性半陰陽を有するSRY negative XX male の1例 - 内性器の検討と成因の考察 - (1997)
    • Prader-Willi症候群とAngelman症候群 (1996)
  • KAWAME Hiroshi ID: 9000000395910

    Articles in CiNii:45

    • Clinical Spectrum and Management of Holoprosencephaly (2000)
    • 真性半陰陽を有するSRY negative XX male の1例 - 内性器の検討と成因の考察 - (1997)
    • Prader-Willi症候群とAngelman症候群 (1996)
  • KAWAME Hiroshi ID: 9000000395910

    Articles in CiNii:45

    • Clinical Spectrum and Management of Holoprosencephaly (2000)
    • 真性半陰陽を有するSRY negative XX male の1例 - 内性器の検討と成因の考察 - (1997)
    • Prader-Willi症候群とAngelman症候群 (1996)
  • Kawame Hiroshi ID: 9000399800484

    Articles in CiNii:1

    • Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare (2019)
  • KAWAME Hiroshi ID: 9000000395910

    Articles in CiNii:45

    • Clinical Spectrum and Management of Holoprosencephaly (2000)
    • 真性半陰陽を有するSRY negative XX male の1例 - 内性器の検討と成因の考察 - (1997)
    • Prader-Willi症候群とAngelman症候群 (1996)
  • KAWAME Hiroshi ID: 9000000860281

    Division of Medical Genetics, Nagano Children's Hospital (2005 from CiNii)

    Articles in CiNii:2

    • Gonadal sex cord stromal tumor in a patient with Rubinstein-Taybi syndrome (2002)
    • Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome (2005)
  • KAWAME Hiroshi ID: 9000001076339

    Department of Genetic Counseling, Ochanomizu University (2011 from CiNii)

    Articles in CiNii:5

    • Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD) : report of a new case and review of the literature (1999)
    • Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia (2005)
    • Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome (2008)
  • KAWAME Hiroshi ID: 9000002017290

    Division of Medical Genetics, Center for Perinatal Medicine, Nagano Children's Hospital (2009 from CiNii)

    Articles in CiNii:2

    • Dichorionic twin fetuses with VACTERL association (2007)
    • Prenatal diagnosis of Holt-Oram syndrome : Role of 3-D ultrasonography (2009)
  • KAWAME Hiroshi ID: 9000238241213

    Division of Medical Genetics, Center for Perinatal Medicine, Nagano Children's Hospital (2010 from CiNii)

    Articles in CiNii:1

    • Prenatal findings in a fetus with contiguous gene syndrome caused by deletion of Xp22.3 that includes locus for X-linked recessive type of chondrodysplasia punctata (CDPX1) (2010)
  • Kawame Hiroshi ID: 9000345403274

    Tohoku Medical Megabank Organization, Tohoku University|Graduate School of Medicine, Tohoku University (2016 from CiNii)

    Articles in CiNii:1

    • The Tohoku Medical Megabank Project: Design and Mission (2016)
  • Kawame Hiroshi ID: 9000399240063

    Articles in CiNii:3

    • 22q11.2欠失症候群の遺伝学 (特集 小児循環器領域の生涯包括遺伝医療) -- (疾患各論) (2019)
    • Genetic counseling for patients and families with lysosomal diseases (2019)
    • Genetic Counseling Role-Play for Medical Education (2005)
  • Kawame Hiroshi ID: 9000404500089

    Department of Education and Training, Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan (2019 from CiNii)

    Articles in CiNii:1

    • Establishment of Integrated Biobank for Precision Medicine and Personalized Healthcare: The Tohoku Medical Megabank Project (2019)
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