Search Results1-20 of  59

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  • Kurosawa Kenji ID: 9000255323919

    Articles in CiNii:1

    • A case report of two brothers with ATR-X syndrome due to low maternal frequency of somatic mosaicism for an intragenic deletion in the ATRX (2014)
  • Kurosawa Kenji ID: 9000322731243

    Articles in CiNii:1

    • SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements (2016)
  • KUROSAWA KENJI ID: 9000001741610

    Department of Pediatrics, Institute of DNA Medicine, Jikei University School of Medicine (1999 from CiNii)

    Articles in CiNii:1

    • Adult-type metachromatic leukodystrophy with a compound heterozygote mutation showing character change and dementia (1999)
  • KUROSAWA Kenji ID: 9000000717298

    群馬県甘楽富岡農業協同組合 (2001 from CiNii)

    Articles in CiNii:1

    • Planned production of vegetables by the direct link between production area and consumers with IT (2001)
  • KUROSAWA Kenji ID: 9000000860276

    Division of Medical Genetics, Clinical Research Institute, Kanagawa Children's Medical Center (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)
  • KUROSAWA Kenji ID: 9000000889828

    Department of Pediatrics, The Jikei University School of Medicine (2001 from CiNii)

    Articles in CiNii:4

    • GENOTYPE-PHENOTYPE CORRELATION IN JAPANESE PATIENTS WITH METACHROMATIC LEUKODYSTROPHY (2001)
    • Molecular analysis of Japanese patients with metachromatic leukodystrophy (1998)
    • Clinical and molecular analysis of Japanese patients with neuronal ceroid lipofuscinosis (1997)
  • KUROSAWA Kenji ID: 9000001076356

    Department of Pediatrics, Tokyo Metropolitan Kita Medical and Rehabilitation Center (1999 from CiNii)

    Articles in CiNii:1

    • 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)
  • KUROSAWA Kenji ID: 9000001260672

    Materials Process Engineering Department Powertrain Production Engineering Division, Nissan Motor Co., Ltd. (2004 from CiNii)

    Articles in CiNii:1

    • Casting CAE for Automotive Parts (2004)
  • KUROSAWA Kenji ID: 9000001733672

    Division of Genetics, Kanagawa Children's Medical Center (2011 from CiNii)

    Articles in CiNii:3

    • Brain MRI findings of older patients with Pallister-Killian syndrome (2006)
    • Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation (2010)
    • 5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infant (2011)
  • KUROSAWA Kenji ID: 9000004870374

    Graduate School of Engineering, Tohoku University (2002 from CiNii)

    Articles in CiNii:1

    • A Method of Multichannel PID Control of 2-Degree of Freedom of Wrist Joint Movements by Functional Electrical Stimulation (2002)
  • KUROSAWA Kenji ID: 9000004948394

    Forensic Science Laboratory, Ishikawa Pref. Police H.Q. (2007 from CiNii)

    Articles in CiNii:7

    • A Study on Modification Method of Stimulation Patterns for FES (1996)
    • Development of a Closed-loop FES System using a 3-D Position and Orientation Sensor (2001)
    • A study on multichannel feedback FES control of the wrist joint (2000)
  • KUROSAWA Kenji ID: 9000005761762

    Articles in CiNii:27

    • 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)
    • The Practice of Genetic Counselling in The Institute for The Severely Handicapped (1999)
  • KUROSAWA Kenji ID: 9000005787217

    Department of Periodontology, Meikai University School of Dentistry (1991 from CiNii)

    Articles in CiNii:1

    • Research into Actual Conditions and Preventive Care in Periodontal Disease : Attempt of Expert-Systems Using Neural-Nets (1991)
  • KUROSAWA Kenji ID: 9000006674657

    Aica Kogyo Company, Limited (2003 from CiNii)

    Articles in CiNii:1

    • 9261 On the Formation and Its Harmony of the Facade in Grand-Place of Brussels (2003)
  • KUROSAWA Kenji ID: 9000017385124

    Department of Medical Genetics, Kanagawa Children's Medical Center (2009 from CiNii)

    Articles in CiNii:1

    • Proximal interstitial 1p36 deletion syndrome : The most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2) (2009)
  • KUROSAWA Kenji ID: 9000017682065

    Forensic Science Laboratory, Ishikawa Pref. Police H.Q. (2009 from CiNii)

    Articles in CiNii:1

    • An Effective Method on Applying Feedback Error Learning Scheme to Functional Electrical Stimulation Controller (2009)
  • KUROSAWA Kenji ID: 9000018281777

    Division of Medical Genetics, Kanagawa Children's Medical Center (2004 from CiNii)

    Articles in CiNii:1

    • No sex differences in 18 trisomy births in the Kanagawa Birth Defects Monitoring Program (2004)
  • KUROSAWA Kenji ID: 9000018282106

    Division of Medical Genetics, Kanagawa Children's Medical Center (2010 from CiNii)

    Articles in CiNii:2

    • Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome : Report of two cases and review of the literature (2009)
    • 1p36 deletion syndrome associated with Prader-Willi-like phenotype (2010)
  • KUROSAWA Kenji ID: 9000021042547

    Articles in CiNii:1

    • Clinical Evaluation of PMG on Gingivitis, Periodontitis and Stomatitis. (1991)
  • KUROSAWA Kenji ID: 9000256574947

    日高西部地区農業改良普及センター (2001 from CiNii)

    Articles in CiNii:1

    • Distribution of Fungicide-Resistant <I>Botrytis cinerea</I> in Hokkaido and Change in the Susceptibility under Plastic House Conditions (2001)
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