Search Results1-20 of  36

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  • Kosaki Kenjiro ID: 9000399800491

    Articles in CiNii:1

    • Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare (2019)
  • KOSAKI KENJIRO ID: 9000001030455

    Division of Medical Genetics, National Center for Child Health and Development (2012 from CiNii)

    Articles in CiNii:17

    • Lymphstasis in a Boy with Noonan Syndrome : Imprication for the Development of Skeletal Features (2003)
    • A JAPANESE PATIENT WITH X-LINKED α-THALASSEMIA/MENTAL RETARDATION SYNDROME : AN ADDITIONAL CASE REPORT (1996)
    • Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia (2005)
  • KOSAKI KENJIRO ID: 9000002099778

    Department of Pediatrics, Keio University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation (2006)
  • KOSAKI KENJIRO ID: 9000257800360

    Department of Pediatrics, Keio University School of Medicine (2003 from CiNii)

    Articles in CiNii:1

    • Lymphstasis in Boy with Noonan Syndrome: Implication for the Development of Skeletal Features (2003)
  • KOSAKI Kenjiro ID: 9000000607528

    Department of Pediatrics, Pharmacia-Upjohn Fund for Growth & Development Research, Keio University School of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Neurodevelopmental toxicity of halogenated aryl hydrocarbons (1999)
  • KOSAKI Kenjiro ID: 9000001803977

    Department of Pediatrics, Keio University School of Medicine, Tokyo, and Department of Human Genetics, Yokohama City University, School of Medicine (2005 from CiNii)

    Articles in CiNii:1

    • Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplication (2005)
  • KOSAKI Kenjiro ID: 9000001999872

    Division of Medical Genetics, Department of Pediatrics, Keio University School of Medicine (2007 from CiNii)

    Articles in CiNii:1

    • Mutational Spectrum of MSUD in the Philippines (2007)
  • KOSAKI Kenjiro ID: 9000018281827

    Department of Pediatrics, Keio University School of Medicine (2004 from CiNii)

    Articles in CiNii:1

    • Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB (2004)
  • KOSAKI Kenjiro ID: 9000018281966

    Department of Pediatrics, Keio University School of Medicine (2007 from CiNii)

    Articles in CiNii:1

    • EFNB1 mutation at the ephrin ligand-receptor dimerization interface in a patient with craniofrontonasal syndrome (2007)
  • KOSAKI Kenjiro ID: 9000256569433

    Department of Pediatrics, School of Medicine, Keio University (2004 from CiNii)

    Articles in CiNii:1

    • Effect of Post-exposure Prophylaxis with Oseltamivir for Those in Contacts with Influenza Patients in Pediatric Wards (2004)
  • KOSAKI Kenjiro ID: 9000257801789

    Department of Pediatrics, Keio University School of Medicine (2006 from CiNii)

    Articles in CiNii:1

    • Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation (2006)
  • KOSAKI Kenjiro ID: 9000364870684

    Articles in CiNii:20

    • Effect of Post-exposure Prophylaxis with Oseltamivir for Those in Contacts with Influenza Patients in Pediatric Wards (2004)
    • Genetic Diagnosis of Retinoblastoma by a Combination of Fluorescence In Situ Hybridization and Restriction Fragment Length Polymorphism (2004)
    • メチル化特異的PCR法を利用する Prader-Willi 症候群, Angelman 症候群の分子遺伝学的診断 (1997)
  • Kenjiro Kosaki ID: 9000408572128

    Articles in CiNii:1

    • A novel missense PTEN mutation identified in a patient with macrocephaly and developmental delay (2019)
  • Kosaki Kenjiro ID: 9000253395774

    慶應義塾大学医学部小児科 (2003 from CiNii)

    Articles in CiNii:1

    • Genetic alterations in gastric preneoplastic lesions-in relation to H. pylori infection-.:in relation to <i>H. pylori</i> infection (2003)
  • Kosaki Kenjiro ID: 9000283362888

    Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan (2014 from CiNii)

    Articles in CiNii:1

    • Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome (2014)
  • Kosaki Kenjiro ID: 9000347188975

    Center for Medical Genetics, Keio University School of Medicine (2017 from CiNii)

    Articles in CiNii:1

    • A Case of Mosaic Tetrasomy 12p (Pallister-Killian Syndrome): Clinical Definition of Hypomelanosis of Ito among Mosaicisms for Abnormal Chromosomes (2017)
  • Kosaki Kenjiro ID: 9000351064786

    Center for Medical Genetics, Keio University School of Medicine (2016 from CiNii)

    Articles in CiNii:1

    • Establishment of Genetic Counseling Office in Municipal Hospital and Efforts for Surveillance of High-risk Patients:- Consideration about the Significance of Genetic Medicine in Familial Tumors Pursued in Municipal Hospital - (2016)
  • Kosaki Kenjiro ID: 9000389555531

    Articles in CiNii:1

    • Tranilast inhibits the expression of genes related to epithelial-mesenchymal transition and angiogenesis in neurofibromin-deficient cells (2018)
  • Kosaki Kenjiro ID: 9000399539616

    Articles in CiNii:1

    • Deep whole-genome sequencing reveals recent selection signatures linked to evolution and disease risk of Japanese (2018)
  • Kosaki Kenjiro ID: 9000399539650

    Articles in CiNii:1

    • IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis (2018)
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