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Volumn 83, Issue 3-4, 1998, Pages 275-280

FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: Results in a translocation carrier, t(5;8)(q33;q13)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 5Q; CHROMOSOME 8Q; CHROMOSOME CHIASM; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION 5; CHROMOSOME TRANSLOCATION 8; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOTE; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; SPERMATOZOON;

EID: 0032454305     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015170     Document Type: Article
Times cited : (60)

References (8)
  • 1
    • 0020560397 scopus 로고
    • Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations
    • Balkan W, Martin RH: Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations. Hum Genet 63:345-348 (1983).
    • (1983) Hum Genet , vol.63 , pp. 345-348
    • Balkan, W.1    Martin, R.H.2
  • 2
    • 0031133236 scopus 로고    scopus 로고
    • Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization
    • Bernardini L, Martini E, Geraedts JPM, Hopman AHN, Lanteri S, Conte N, Capitanio GL: Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization. Mol hum Reprod 3:431-438 (1997).
    • (1997) Mol Hum Reprod , vol.3 , pp. 431-438
    • Bernardini, L.1    Martini, E.2    Geraedts, J.P.M.3    Hopman, A.H.N.4    Lanteri, S.5    Conte, N.6    Capitanio, G.L.7
  • 3
    • 0022908388 scopus 로고
    • Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21)
    • Gabriel-Robez O, Ratomponirina C, Dutrillaux B, Carré-Pigeon F, Rumpier Y: Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21). Cytogenet Cell Genet 43:154-160 (1986).
    • (1986) Cytogenet Cell Genet , vol.43 , pp. 154-160
    • Gabriel-Robez, O.1    Ratomponirina, C.2    Dutrillaux, B.3    Carré-Pigeon, F.4    Rumpier, Y.5
  • 4
    • 0027472131 scopus 로고
    • Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: Quadrivalent configuration, orientation and first meiotic segregation
    • Goldman A, Hultén M: Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: quadrivalent configuration, orientation and first meiotic segregation. Chromosoma 102:102-111 (1993b).
    • (1993) Chromosoma , vol.102 , pp. 102-111
    • Goldman, A.1    Hultén, M.2
  • 5
    • 0025063097 scopus 로고
    • Sperm chromosome analysis in a man heterozygous for a reciprocal translocation, 46,XY, t(12;20)(q24.3;q11)
    • Martin RH, McGillivray B, Barclay L, Hildebrand K, Ko E: Sperm chromosome analysis in a man heterozygous for a reciprocal translocation, 46,XY, t(12;20)(q24.3;q11). Hum Reprod 5:606-609 (1990b).
    • (1990) Hum Reprod , vol.5 , pp. 606-609
    • Martin, R.H.1    McGillivray, B.2    Barclay, L.3    Hildebrand, K.4    Ko, E.5
  • 6
    • 0028855742 scopus 로고
    • Sperm chromosome complements in a man heterozygous for a reciprocal translocation, 46,XY, t(9;13)(q21.1;q21.2), and a review of the literature
    • Martin RH, Spriggs E: Sperm chromosome complements in a man heterozygous for a reciprocal translocation, 46,XY, t(9;13)(q21.1;q21.2), and a review of the literature. Clin Genet 47:42-46 (1995).
    • (1995) Clin Genet , vol.47 , pp. 42-46
    • Martin, R.H.1    Spriggs, E.2
  • 7
    • 0001149670 scopus 로고
    • Detection by fluorescence in situ hybridization of chromosome 7, 11, 12, 18, X and Y abnormalities from oligoasthenoteratozoospermic patients of an in vitro fertilization programme
    • Pang MG, Zackowski JL, Hoegerman SF, Moon SY, Cuticchia AJ, Costa AA, Kearns WG: Detection by fluorescence in situ hybridization of chromosome 7, 11, 12, 18, X and Y abnormalities from oligoasthenoteratozoospermic patients of an in vitro fertilization programme. J assist Reprod Genet 12 (Suppl):53S (1995).
    • (1995) J Assist Reprod Genet , vol.12 , Issue.SUPPL.
    • Pang, M.G.1    Zackowski, J.L.2    Hoegerman, S.F.3    Moon, S.Y.4    Cuticchia, A.J.5    Costa, A.A.6    Kearns, W.G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.