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Journal Abstract Search

119 related items for PubMed ID: 2757357

  • 1. [Nucleolus organizer region--centromere translocation].
    de Blois MC, Rethoré MO, Lejeune J.
    Ann Genet; 1989; 32(2):106-8. PubMed ID: 2757357
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  • 4. Subfertile couple with t(4;22)(q23;q11.2).
    Srebniak M, Popowska L, Wawrzkiewicz-Witkowska A, Tomaszewska A, Kazmierczak W.
    J Appl Genet; 2005; 46(3):333-6. PubMed ID: 16110194
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  • 5. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.
    Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M.
    Prenat Diagn; 1999 Mar; 19(3):282-6. PubMed ID: 10210132
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  • 7. [Karyotype of the parents after spontaneous abortion? Translocation 46 XY t (2p-;21q +) detected in the husband of a woman who presented with 2 early spontaneous abortions].
    Rabineau D, Zorn JR, Girard S, Salesses A.
    J Gynecol Obstet Biol Reprod (Paris); 1974 Mar; 3(2):265-70. PubMed ID: 4470572
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  • 8. Cytogenetic analysis in 61 couples with spontaneous abortions.
    Jiang J, Fu M, Wang D.
    Chin Med J (Engl); 2001 Feb; 114(2):200-1. PubMed ID: 11780207
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  • 9. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
    Knegt AC, Li S, Engelen JJ, Bijlsma EK, Warburton PE.
    Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
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  • 11. [The functional characteristics of the chromosomal nucleolus organizer regions of patients with endometrial cancer].
    Buchinskaia LG, Polishchuk LZ, Ganina KP.
    Tsitol Genet; 1995 Mar; 29(4):32-7. PubMed ID: 8604524
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  • 14. Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.
    Pazarbaşi A, Demirhan O, Turgut M, Güzel I, Taştemir D.
    Genet Couns; 2008 Mar; 19(3):301-8. PubMed ID: 18990986
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  • 15. Balanced X;15 translocation 46,X,t(X;15)(q21;q23) associated with primary amenorrhea.
    Ji XW, Chen XY, Tan J, Liang H.
    Am J Med Genet; 1988 Dec; 31(4):783-6. PubMed ID: 3239568
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  • 16. Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.
    Varley JM, Gosden J, Hultén M.
    Hum Genet; 1981 Dec; 59(4):422-8. PubMed ID: 6174409
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  • 18. NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome.
    Daniel A, Ekblom L, Phillips S, FitzGerald JM, Opitz JM.
    Am J Med Genet; 1985 Nov; 22(3):577-84. PubMed ID: 4061490
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