Search Results1-20 of  27

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  • Kurahashi Hiroki ID: 9000009560097

    Articles in CiNii:1

    • Refined Mapping of Eight Cosmid Markers on Human Chromosome 22 (1994)
  • Kurahashi Hiroki ID: 9000322731306

    Articles in CiNii:1

    • Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother (2016)
  • Kurahashi Hiroki ID: 9000331880346

    Articles in CiNii:1

    • A PDE3A mutation in familial hypertension and brachydactyly syndrome (2016)
  • KURAHASHI Hiroki ID: 9000000767437

    Division of Clinical Genetics, Department of Medical Genetics, B9 Biomedical Research Center, Osaka University Medical School (1998 from CiNii)

    Articles in CiNii:1

    • Identification of the Disease Causing Gene by Positional Cloning (1998)
  • KURAHASHI Hiroki ID: 9000001076638

    Division of Clinical Genetics, Department of Medical Genetics, Biomedical Research Center, Faculty of Medicine, Osaka University (1999 from CiNii)

    Articles in CiNii:1

    • Mutation analysis of Japanese patient with fucosidosis (1999)
  • KURAHASHI Hiroki ID: 9000001082555

    Division of Clinical Genetics, Department of Medical Genetics, Biomedical Research Center, Osaka University Medical School (1998 from CiNii)

    Articles in CiNii:1

    • Novel polymorphisms in the βig-h3 gene (1998)
  • KURAHASHI Hiroki ID: 9000001362932

    Division of Clinical Genetics, Department of Medical Genetics, Biomedical Research Center, Osaka University Medical School (1997 from CiNii)

    Articles in CiNii:1

    • DUAL-COLOR FISH ANALYSIS OF BREAKPOINTS ON ROBERTSONIAN TRANSLOCATIONS (1997)
  • KURAHASHI Hiroki ID: 9000002130326

    21st Century COE Program, Development Center for Targeted and Minimally Invasive Diagnosis and Treatment (2008 from CiNii)

    Articles in CiNii:1

    • Mouse model for allogeneic immune reaction against fetus recapitulates human pre-eclampsia (2008)
  • KURAHASHI Hiroki ID: 9000004392539

    Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University (2012 from CiNii)

    Articles in CiNii:8

    • Isolated Iissencephaly sequence with balanced chromosome translocation involving 17p13.3 (1998)
    • Low Grade Amplification of MDM2 Gene in a Subset of Human Breast Cancers without p53 Alterations (1994)
    • Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome (1999)
  • KURAHASHI Hiroki ID: 9000019185726

    The Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University (2012 from CiNii)

    Articles in CiNii:3

    • Mechanism of complex gross chromosomal rearrangements : A commentary on Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation (2012)
    • Recent advance in our understanding of the molecular nature of chromosomal abnormalities (2009)
    • Screening of genes involved in chromosome segregation during meiosis I : toward the identification of genes responsible for infertility in humans (2010)
  • KURAHASHI Hiroki ID: 9000255895988

    Department of Pediatrics, Osaka University Hospital (1992 from CiNii)

    Articles in CiNii:1

    • Short-Term Intensive Therapy for B Cell Lymphoma. (1992)
  • KURAHASHI Hiroki ID: 9000256378389

    Division of Clinical Genetics, Department of Medical Genetics, B9 Biomedical Research Center, Osaka University Medical School (1998 from CiNii)

    Articles in CiNii:1

    • Identification of the Disease Causing Gene by Positional Cloning. (1998)
  • KURAHASHI Hiroki ID: 9000256645078

    Department of Pediatrics, Osaka University School of Medicine (1992 from CiNii)

    Articles in CiNii:1

    • Genotypic Typing Using Amplified Variable Number of Tandem Repeats with Polymerase Chain Reaction Following Allogeneic Bone Marrow Transplantation. (1992)
  • KURAHASHI Hiroki ID: 9000256645204

    Division of Clinical Genetics, Department of Medical Genetics, Biological Research Center, Osaka University Medical School (1993 from CiNii)

    Articles in CiNii:1

    • Immunological Phenotype and Prognosis of T-Lineage Malignancy in Children. (1993)
  • KURAHASHI Hiroki ID: 9000256645649

    Department of Pediatrics, Osaka University School of Medicine (1994 from CiNii)

    Articles in CiNii:1

    • Allogeneic Bone Marrow Transplantation in an Infant with Chronic Myelomonocytic Leukemia. (1994)
  • KURAHASHI Hiroki ID: 9000283528686

    Department of Pediatrics, Osaka University Hospital (1986 from CiNii)

    Articles in CiNii:1

    • Heterogeneity of Tγ-Lymphoproliferative Disorder:—A Case Report and a Review of Literature— (1986)
  • KURAHASHI Hiroki ID: 9000345371389

    藤田保健衛生大学総合医科学研究所 分子遺伝学研究部門 (2017 from CiNii)

    Articles in CiNii:1

    • Genomic medicine and genetic counseling (2017)
  • Kurahashi Hiroki ID: 9000019155566

    龍谷大学法学研究科修士課程修了 (2012 from CiNii)

    Articles in CiNii:1

    • Local Government and Traditional Leadership in South Africa (2012)
  • Kurahashi Hiroki ID: 9000256857065

    The Department of Pediatrics, Osaka University School of Medicine (1988 from CiNii)

    Articles in CiNii:1

    • A case of idiopathic hypertophic cardiomyopathy involving the right ventricle (1988)
  • Kurahashi Hiroki ID: 9000257806399

    Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake 470-1192, Japan (2014 from CiNii)

    Articles in CiNii:1

    • A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis (2014)
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