Search Results1-13 of  13

  • KONDOH Tatsuro ID: 9000001369233

    Department of Pediatrics, Nagasaki University School of Medicine （2002 from CiNii）

    Articles in CiNii:1

    • Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection （2002）
  • KONDOH Tatsuro ID: 9000006121925

    Nagasaki Junshin Catholic University （2005 from CiNii）

    Articles in CiNii:1

    • Current State and Problems of Genetic Counseling in Nagasaki Prefecture （2005）
  • KONDOH Tatsuro ID: 9000014281126

    Division of Developmental Disabilities, Misakaenosono Mutsumi, The institute for Persons with severe Intellectual/Motor Disabilities （2008 from CiNii）

    Articles in CiNii:1

    • Fraternal Cases of Hypohidrotic Ectodermal Dysplasia （2008）
  • KONDOH Tatsuro ID: 9000256641541

    Department of Pediatrics, Nagasaki University School of Medicine （1996 from CiNii）

    Articles in CiNii:1

    • Prolonged Recovery of Hematopoiesis after BMT in a Case of Severe Aplastic Anemia. （1996）
  • KONDOH Tatsuro ID: 9000257940705

    Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences|Division of Developmental Disabilities, Misakaenosono Mutsumi, The institute for Persons with severe Intellectual/Motor Disabilities （2008 from CiNii）

    Articles in CiNii:1

    • Fraternal Cases of Hypohidrotic Ectodermal Dysplasia （2008）
  • Kishino Tatsuya ID: 9000002217256

    Department of Otolaryngology-Head and Neck Surgery, Tohoku University School of Medicine （2012 from CiNii）

    Articles in CiNii:85

    • Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women （2000）
    • A case of megalocornea-mental retardation syndrome complicated with bilateral sensorineural hearing impairment （1999）
    • A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia （2000）
  • Kondoh Tatsuro ID: 9000022764059

    Articles in CiNii:1

    • Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in Japan. （2008）
  • Kondoh Tatsuro ID: 9000023245233

    Articles in CiNii:1

    • Four Novel NIPBL Mutations in Japanese Patients With Cornelia de Lange Syndrome （2005）
  • Kondoh Tatsuro ID: 9000024214823

    Articles in CiNii:1

    • Familial brain arteriovenous malformation maps to 5p13-q14, 15q11-q13 or 18p11: linkage analysis with clipped fingernail DNA on high-density SNP array. （2010）
  • Kondoh Tatsuro ID: 9000283424279

    The Misakaenosono Mutsumi Developmental, Medical and Welfare Center （2014 from CiNii）

    Articles in CiNii:1

    • The relationship between physical signs of aging and social functioning in persons with Down syndrome in Japan （2014）
  • Kondoh Tatsuro ID: 9000369353700

    Articles in CiNii:1

    • Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver–Russell syndrome （2017）
  • Kondoh Tatsuro ID: 9000402231593

    Articles in CiNii:1

    • A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome （2018）
  • Tatsuro Kondoh ID: 9000002216709

    Department of Pediatrics, Nagasaki University School of Medicine （1997 from CiNii）

    Articles in CiNii:1

    • -Review Article- Children with Chronic Granulomatous Disease （1997）
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