Kanagawa Children's Medical Center View Homepage

Ontology type: grid:Healthcare  | foaf:Organization     

Organization Info

Publications in SciGraph latest 20 shown

  • 2019-12 Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions in CLINICAL EPIGENETICS
  • 2019-12 A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation in HUMAN GENOME VARIATION
  • 2019-05 Nonsense variants in STAG2 result in distinct sex-dependent phenotypes in JOURNAL OF HUMAN GENETICS
  • 2019-04-09 Correction to: A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging features. in JOURNAL OF NEUROLOGY
  • 2019-04 Hematopoietic stem cell transplantation in children and adolescents with relapsed or refractory B-cell non-Hodgkin lymphoma in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2019-03-19 A cluster of disseminated small cortical lesions in MELAS: its distinctive clinical and neuroimaging features in JOURNAL OF NEUROLOGY
  • 2019-03 Allogeneic hematopoietic stem cell transplantation for children and adolescents with high-risk cytogenetic AML: distinctly poor outcomes of FUS-ERG-positive cases in BONE MARROW TRANSPLANTATION
  • 2019-02-19 Transcanalicular endoscopic primary dacryoplasty for congenital nasolacrimal duct obstruction in EYE
  • 2019-02-04 Hematopoietic stem-cell transplantation in children with refractory acute myeloid leukemia in BONE MARROW TRANSPLANTATION
  • 2019-02 Bilateral breast reconstruction and pectus excavatum correction: a case and review of the literature in EUROPEAN JOURNAL OF PLASTIC SURGERY
  • 2019-01 Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes in HUMAN GENETICS
  • 2018-12 Mitochondrial DNA 3243A>T mutation in a patient with MELAS syndrome in HUMAN GENOME VARIATION
  • 2018-12 Secondary cancer after a childhood cancer diagnosis: viewpoints considering primary cancer in INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY
  • 2018-12 Nonsyndromic intellectual disability with novel heterozygous SCN2A mutation and epilepsy in HUMAN GENOME VARIATION
  • 2018-12 Biallelic mutations of EGFR in a compound heterozygous state cause ectodermal dysplasia with severe skin defects and gastrointestinal dysfunction in HUMAN GENOME VARIATION
  • 2018-12 Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly in HUMAN GENOME VARIATION
  • 2018-12 Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese in SCIENTIFIC REPORTS
  • 2018-12 KMT2A-rearranged infantile acute myeloid leukemia masquerading as juvenile myelomonocytic leukemia in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2018-11-23 RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathy in GENETICS IN MEDICINE
  • 2018-11 Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion in JOURNAL OF HUMAN GENETICS
  • JSON-LD is the canonical representation for SciGraph data.

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    Download the RDF metadata as:  json-ld nt turtle xml License info


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    curl -H 'Accept: application/ld+json' 'https://www.grid.ac/institutes/grid.414947.b'

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    This table displays all metadata directly associated to this object as RDF triples.

    12 TRIPLES      11 PREDICATES      12 URIs      5 LITERALS

    Subject Predicate Object
    1 grid-institutes:grid.414947.b sgo:sdDataset grid
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    5 grid:id grid.414947.b
    6 grid:isni 0000 0004 0377 7528
    7 grid:wikipediaPage https://en.wikipedia.org/wiki/Kanagawa_Children%27s_Medical_Center
    8 rdf:type grid:Healthcare
    9 foaf:Organization
    10 rdfs:label Kanagawa Children's Medical Center
    11 skos:prefLabel Kanagawa Children's Medical Center
    12 foaf:homepage http://kcmc.kanagawa-pho.jp/about/greeting_en.html

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