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Journal Abstract Search

199 related items for PubMed ID: 9147886

  • 21. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE, Kooper AJ, Winarni TI, Smits AP, Faradz SM, Hamel BC.
    Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036
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  • 22. Inheritance of imbalances in recurrent chromosomal translocation t(11;22): clarification by PGT-SR and sperm-FISH analysis.
    Zenagui R, Bernicot I, Ranisavljevic N, Haquet E, Ferrieres-Hoa A, Pellestor F, Anahory T.
    Reprod Biomed Online; 2019 Jul; 39(1):40-48. PubMed ID: 31097322
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  • 24. 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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  • 27. An unbalanced translocation 46,XX,+der(18)t(18;21)(q12.2;q11.2)mat,-21 associated with maternal isodisomy 18pter-->18q12.2.
    de Ravel TJ, Matthijs G, Fryns J.
    Ann Genet; 2001 May; 44(2):63-6. PubMed ID: 11522242
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  • 29. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
    Wang H, McLaughlin M, Thompson C, Hunter AG.
    Am J Med Genet; 1993 Jun 15; 46(5):559-62. PubMed ID: 8322821
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  • 36. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.
    Smeets D, van Ravenswaaij C, de Pater J, Gerssen-Schoorl K, Van Hemel J, Janssen G, Smits A.
    J Med Genet; 1997 Jan 15; 34(1):18-23. PubMed ID: 9032644
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  • 40. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
    Batista DA, Pai GS, Stetten G.
    Am J Med Genet; 1994 Nov 15; 53(3):255-63. PubMed ID: 7856662
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