Search Results1-11 of  11

  • Niihori Tetsuya ID: 9000314400660

    Articles in CiNii:1

    • Recent advances in RASopathies (Special Issue : Cardiovascular Genetics) （2016）
  • Niihori Tetsuya ID: 9000326638159

    Articles in CiNii:1

    • Human genetic variation database, a reference database of genetic variations in the Japanese population （2016）
  • NIIHORI Tetsuya ID: 9000238239870

    Department of Medical Genetics, Tohoku University School of Medicine （2011 from CiNii）

    Articles in CiNii:1

    • A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder （2011）
  • NIIHORI Tetsuya ID: 9000258015725

    Department of Medical Genetics, Tohoku University Graduate School of Medicine （2014 from CiNii）

    Articles in CiNii:1

    • Search for novel pancreatitis-associated genes （2014）
  • NIIHORI Tetsuya ID: 9000261041304

    Department of Medical Genetics, Tohoku University School of Medicine （2013 from CiNii）

    Articles in CiNii:1

    • Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure （2013）
  • NIIHORI Tetsuya ID: 9000317563026

    Department of Medical Genetics, Tohoku University Graduate School of Medicine （2016 from CiNii）

    Articles in CiNii:1

    • Application of targeted next generation sequencing for the comprehensive analysis of pancreatitis susceptibility genes （2016）
  • NIIHORI Tetsuya ID: 9000345371404

    東北大学大学院医学系研究科遺伝医療学分野 （2017 from CiNii）

    Articles in CiNii:1

    • Novel causative gene for radioulnar synostosis with amegakaryocytic thrombocytopenia （2017）
  • NIIHORI Tetsuya ID: 9000410151357

    Department of Medical Genetics, Tohoku University School of Medicine （2020 from CiNii）

    Articles in CiNii:1

    • LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases （2020）
  • Niihori Tetsuya ID: 9000401560093

    Department of Medical Genetics; Tohoku University School of Medicine; Sendai Japan （2017 from CiNii）

    Articles in CiNii:1

    • Patient with a novel purine-rich element binding protein A mutation:A novel PURA mutation （2017）
  • Niihori Tetsuya ID: 9000405634614

    Department of Medical Genetics, Tohoku University School of Medicine, Sendai, Miyagi 980-8574, Japan （2019 from CiNii）

    Articles in CiNii:1

    • Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome （2019）
  • OGAWA TAKENORI ID: 9000005957047

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

    Articles in CiNii:22

    • A Case Report of Sinonasal Teratocarcinosarcoma （2000）
    • Long-Term Follow-up of Obstructive Sleep Apnea Syndrome Following Surgery in Children and Adults （2000）
    • Allelic Loss Correlated with Tissue Specificity in Head and Neck Squamous Cell Carcinomas and the Clinical Features of Patients （2004）
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