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Journal Abstract Search


106 related items for PubMed ID: 1427783

  • 21. Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11).
    Estop AM, Cieply KM, Munne S, Feingold E.
    Hum Genet; 1999 May; 104(5):412-7. PubMed ID: 10394934
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  • 22. Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH.
    Martini E, von Bergh AR, Coonen E, de Die-Smulders CE, Hopman AH, Ramaekers FC, Geraedts JP.
    Hum Genet; 1998 Feb; 102(2):157-65. PubMed ID: 9521583
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  • 23. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.
    Jobanputra V, Chung WK, Hacker AM, Emanuel BS, Warburton D.
    Prenat Diagn; 2005 Aug; 25(8):683-6. PubMed ID: 16049998
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  • 24. Fine mapping of the constitutional translocation t(11;22)(q23;q11).
    Tapia-Páez I, O'Brien KP, Kost-Alimova M, Sahlén S, Kedra D, Bruder CE, Andersson B, Roe BA, Hu P, Imreh S, Blennow E, Dumanski JP.
    Hum Genet; 2000 May; 106(5):506-16. PubMed ID: 10914680
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  • 25. [Translocation 11q;22q: a clinico-cytogenetic study].
    Lur'e IV, Rumiantseva NV, Podleshchuk LV, Kozlova SI, Kulak VD, Naumchik IV, Gorelik LB, Zolotukhina TV, Kuznetsov MI.
    Genetika; 1992 Oct; 28(10):129-35. PubMed ID: 1468637
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  • 26. Meiotic segregation study of a novel t(3;6)(q21;q23) in an infertile man using fluorescence in situ hybridization (FISH).
    Mokánszki A, Ujfalusi A, Balogh E, Sümegi A, Antal-Szalmás P, Bazsáné ZK, Molnár Z, Varga A, Sápy T, Jakab A, Oláh É.
    Syst Biol Reprod Med; 2012 Jun; 58(3):160-4. PubMed ID: 22540876
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  • 27. Re: G. Cimino et al., Cloning of ALL-1, the locus involved in leukemias with the t(4;11)(q21;q23), t(9;11)(p22;q23), and t(11;19)(q23;p13) chromosome translocations. Cancer Res., 51: 6712-6714, 1991.
    Rowley JD, Diaz MO.
    Cancer Res; 1992 May 15; 52(10):2999. PubMed ID: 1581914
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  • 29. Gamete segregation in female carriers of Robertsonian translocations.
    Munné S, Escudero T, Sandalinas M, Sable D, Cohen J.
    Cytogenet Cell Genet; 2000 May 15; 90(3-4):303-8. PubMed ID: 11124538
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  • 40. Prenatal diagnosis of supernumerary chromosome derivative (22) due to maternal balanced translocation in association with diaphragmatic hernia: a case report.
    Kadir RA, Hastings R, Economides DL.
    Prenat Diagn; 1997 Aug 15; 17(8):761-4. PubMed ID: 9267900
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