Yoshikazu Kuroki


Ontology type: schema:Person     


Person Info

NAME

Yoshikazu

SURNAME

Kuroki

Publications in SciGraph latest 50 shown

  • 2011-10 HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome in JOURNAL OF HUMAN GENETICS
  • 1998-12 Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion in EUROPEAN JOURNAL OF PEDIATRICS
  • 1995-12 Anal atresia: Effect of smoking and drinking habits during pregnancy in JOURNAL OF HUMAN GENETICS
  • 1994-06 Asphyxiating thoracic dystrophy: Surgical correction and 2-year follow-up in a girl in JOURNAL OF HUMAN GENETICS
  • 1994-03 Metacarpophalangeal pattern profile analysis in 14 Japanese children with Sotos syndrome in JOURNAL OF HUMAN GENETICS
  • 1992-11 DNA analyses of XX and XX-hypospadiac males in HUMAN GENETICS
  • 1991-06 DNA analysis of a patient with two different marker chromosomes using Y-specific DNA probes in JOURNAL OF HUMAN GENETICS
  • 1990-12 Two unrelated cases of single maxillary central incisor with 7q terminal deletion in JOURNAL OF HUMAN GENETICS
  • 1989-05 Family study of common fragile sites in HUMAN GENETICS
  • 1987-10 Familial retinoblastoma (mother and son) with 13q14 deletion in HUMAN GENETICS
  • 1987-06 Activity and antigen of coagulation factors VII and X in five patients with abnormal chromosome 13 in JOURNAL OF HUMAN GENETICS
  • 1987-03 Partial distal 12q trisomy with arachnoid cyst in JOURNAL OF HUMAN GENETICS
  • 1986-02 Are Down syndrome patients predisposed to Moyamoya disease? in EUROPEAN JOURNAL OF PEDIATRICS
  • 1984-09 A female infant with pure duplication 12q24.2→qter in JOURNAL OF HUMAN GENETICS
  • 1984-06 Predisposition to autoimmune thyroiditis in ring chromosome 18 syndrome in JOURNAL OF HUMAN GENETICS
  • 1984-03 The Prader-Willi syndrome and interstitial deletion of chromosome 15: High-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants in JOURNAL OF HUMAN GENETICS
  • 1984-03 A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22) in JOURNAL OF HUMAN GENETICS
  • 1983-09 Down syndrome with 45 chromosomes in JOURNAL OF HUMAN GENETICS
  • 1983-07 Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46,XY or XX,del(8)(q23.3q24.13) in HUMAN GENETICS
  • 1982-12 Ring 18 mosaicism in identical twins in HUMAN GENETICS
  • 1981-03 Trisomy 18q in HUMAN GENETICS
  • 1980-12 The “happy puppet” syndrome in two siblings in HUMAN GENETICS
  • 1980-07 A case of r(21) with stigmata of atypical Down syndrome in HUMAN GENETICS
  • 1980-05 Cerebro-costo-mandibular syndrome in HUMAN GENETICS
  • 1979-10 Partial trisomy of 11 and 22 due to familial translocation t(11;22) (q23;q11), inherited in three generations in HUMAN GENETICS
  • 1979-01 A case of 21q-syndrome with normal SOD-1 activity in HUMAN GENETICS
  • 1977-01 A case of 9p- syndrome in HUMAN GENETICS
  • 1975-03 A 6p trisomy detected in a family with a “giant satellite” in HUMANGENETIK
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