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Volumn 89, Issue 2, 1996, Pages 170-172

Familial supernumerary chromosome and malignancy

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CANCER SCREENING; CANCER SUSCEPTIBILITY; CARCINOGENESIS; CASE REPORT; CHROMOSOME 15; GENETIC SUSCEPTIBILITY; GLIOMA; HUMAN; LEUKEMIA; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SUPERNUMERARY CHROMOSOME; THYROID CANCER;

EID: 0030586206     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-4608(96)00069-6     Document Type: Article
Times cited : (4)

References (12)
  • 1
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    • 1. Ferguson-Smith MA, Yates JRW (1984): Maternal age specific rates for chromosome aberrations and factors influencing them: Report of a collaborative European study on 52,965 amniocenteses. Prenat Diagn 4:5-44.
    • (1984) Prenat Diagn , vol.4 , pp. 5-44
    • Ferguson-Smith, M.A.1    Yates, J.R.W.2
  • 2
    • 0025941775 scopus 로고
    • De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints
    • 2. Warburton D (1991): De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: Clinical significance and distribution of breakpoints. Amer J Hum Genet 49:995-1013.
    • (1991) Amer J Hum Genet , vol.49 , pp. 995-1013
    • Warburton, D.1
  • 3
    • 0021331411 scopus 로고
    • Mosaic inversion duplication of 15 without phenotypic effect: Occurrence in father and daughter
    • 3. Knight LA, Lipson M, Mann J, Bachman R (1984): Mosaic inversion duplication of 15 without phenotypic effect: Occurrence in father and daughter. Am J Med Genet 17:649-654.
    • (1984) Am J Med Genet , vol.17 , pp. 649-654
    • Knight, L.A.1    Lipson, M.2    Mann, J.3    Bachman, R.4
  • 4
    • 0021917574 scopus 로고
    • Forty-four probands with an additional "marker" chromosome
    • 4. Buckton KE, Spowart G, Newton MS, and Evans HJ (1985): Forty-four probands with an additional "marker" chromosome. Hum Genet 69:353-370.
    • (1985) Hum Genet , vol.69 , pp. 353-370
    • Buckton, K.E.1    Spowart, G.2    Newton, M.S.3    Evans, H.J.4
  • 5
    • 0025669945 scopus 로고
    • Nonrandom chromosome abnormalities in testicular and ovarian germ cell tumor cell lines
    • 5. Murty VVVS, Dmitrovsky E, Bosl GJ, Chaganti RSK (1990): Nonrandom chromosome abnormalities in testicular and ovarian germ cell tumor cell lines. Canc Genet Cytogenet 50(1):67-73.
    • (1990) Canc Genet Cytogenet , vol.50 , Issue.1 , pp. 67-73
    • Murty, V.V.V.S.1    Dmitrovsky, E.2    Bosl, G.J.3    Chaganti, R.S.K.4
  • 6
    • 0019325857 scopus 로고
    • Controlled silver staining of nucleolus organizer regions with a protective colloidal developer: A 1-step method
    • 6. Howell WM and Black DA (1980): Controlled silver staining of nucleolus organizer regions with a protective colloidal developer: A 1-step method. Experientia 36:1014-1015.
    • (1980) Experientia , vol.36 , pp. 1014-1015
    • Howell, W.M.1    Black, D.A.2
  • 7
    • 0018331061 scopus 로고
    • The mechanism of C-banding. Depurination and B-elimination
    • 7. Holmquist G (1979): The mechanism of C-banding. Depurination and B-elimination. Chromosoma 72:203-224.
    • (1979) Chromosoma , vol.72 , pp. 203-224
    • Holmquist, G.1
  • 8
    • 0026920425 scopus 로고
    • Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-q13) by YAC cloning and FISH analysis
    • 8. Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, et al (1992): Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-q13) by YAC cloning and FISH analysis. Hum Mol Genet 1:417-425.
    • (1992) Hum Mol Genet , vol.1 , pp. 417-425
    • Kuwano, A.1    Mutirangura, A.2    Dittrich, B.3    Buiting, K.4    Horsthemke, B.5    Saitoh, S.6    Niikawa, N.7
  • 9
    • 0002232454 scopus 로고
    • Prenatal diagnosis of chromosome abnormalities
    • Milunsky A (Ed). New York: Plenum Press
    • 9. Hsu LYS. Prenatal diagnosis of chromosome abnormalities. In Milunsky A (Ed). Genetic Disorders and the Fetus. New York: Plenum Press, 1992: 155-210.
    • (1992) Genetic Disorders and the Fetus , pp. 155-210
    • Hsu, L.Y.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.