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Volumn 88, Issue 9, 1999, Pages 1040-1043

Ring chromosome 17 syndrome with monosomy 17 mosaicism: Case report and literature review

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 17; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; CRANIOFACIAL MALFORMATION; CYTOGENETICS; HUMAN; JAPAN; KARYOTYPE; MALE; MONOSOMY; NEWBORN; PRIORITY JOURNAL; RING CHROMOSOME;

EID: 0032852140     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/08035259950168595     Document Type: Article
Times cited : (6)

References (12)
  • 3
    • 0019435755 scopus 로고
    • An infant with ring 17 chromosome and unusual dermatoglyphs: A new syndrome?
    • Carpenter NJ, Leichtman LG, Stamper S, Say B. An infant with ring 17 chromosome and unusual dermatoglyphs: A new syndrome? Med Genet 1981; 18: 234-6
    • (1981) Med Genet , vol.18 , pp. 234-236
    • Carpenter, N.J.1    Leichtman, L.G.2    Stamper, S.3    Say, B.4
  • 4
    • 0020034570 scopus 로고
    • Ring chromosome 17 in a mentally retarded young man - Clinical, cytogenic, and biochemical investigations
    • Chudley AE, Pabello PD, McAlpine PJ, Nickel BE, Shokeir MHK. Ring chromosome 17 in a mentally retarded young man - Clinical, cytogenic, and biochemical investigations. Am J Med Genet 1982; 12: 219-25
    • (1982) Am J Med Genet , vol.12 , pp. 219-225
    • Chudley, A.E.1    Pabello, P.D.2    McAlpine, P.J.3    Nickel, B.E.4    Shokeir, M.H.K.5
  • 8
  • 9
    • 0027506860 scopus 로고
    • Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NFI)
    • Wiktor A, Van Dyke DI., Weiss L. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NFI). Am J Med Genet 1993; 45: 22-4
    • (1993) Am J Med Genet , vol.45 , pp. 22-24
    • Wiktor, A.1    Van Dyke, D.I.2    Weiss, L.3
  • 11
    • 0031012229 scopus 로고    scopus 로고
    • Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation
    • Morrison PJ, Smith NM, Martin KE, Young ID. Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation. Am J Meal Genet 1997; 68: 50-3
    • (1997) Am J Meal Genet , vol.68 , pp. 50-53
    • Morrison, P.J.1    Smith, N.M.2    Martin, K.E.3    Young, I.D.4
  • 12
    • 0019800346 scopus 로고
    • The cytogenetic and clinical implications of a ring chromosome 2
    • Cote GB, Katsantonia A, Deligeorgis D. The cytogenetic and clinical implications of a ring chromosome 2. Ann Genet 1981; 24: 231-5
    • (1981) Ann Genet , vol.24 , pp. 231-235
    • Cote, G.B.1    Katsantonia, A.2    Deligeorgis, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.