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Journal Abstract Search

383 related items for PubMed ID: 8950677

  • 21. 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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  • 22. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH, Cho HS, Lee ES, Jung BC.
    Korean J Lab Med; 2010 Jun 15; 30(3):312-7. PubMed ID: 20603594
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  • 26. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.
    Simi P, Ceccarelli M, Barachini A, Floridia G, Zuffardi O.
    Hum Genet; 1992 Feb 15; 88(4):482-3. PubMed ID: 1740326
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  • 29. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 15; 41(5):367-71. PubMed ID: 8725766
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  • 30. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
    Mishra R, Paththinige CS, Sirisena ND, Nanayakkara S, Kariyawasam UGIU, Dissanayake VHW.
    BMC Pediatr; 2018 Jan 08; 18(1):4. PubMed ID: 29310616
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  • 31. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
    Murthy DS, Patel ZM, Ambani LM.
    Clin Genet; 1980 Oct 08; 18(4):233-8. PubMed ID: 7438504
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  • 33. Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation.
    Chen CP, Lin SP, Hsu CH, Chern SR, Su JW, Chen YJ, Pan CW, Wang W.
    Genet Couns; 2012 Oct 08; 23(2):223-9. PubMed ID: 22876581
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  • 35. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Oct 08; 19(2):199-209. PubMed ID: 18618995
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  • 36. Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization.
    Estop AM, Cieply KM, Wakim A, Feingold E.
    Cytogenet Cell Genet; 1998 Oct 08; 83(3-4):193-8. PubMed ID: 10072576
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  • 38. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype.
    Yamamoto K, Hato A, Minagawa K, Yakushijin K, Urahama N, Gomyo H, Sada A, Okamura A, Ito M, Matsui T.
    Cancer Genet Cytogenet; 2004 Nov 08; 155(1):67-73. PubMed ID: 15527905
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  • 39. Molecular studies of translocations and trisomy involving chromosome 13.
    Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA.
    Am J Med Genet; 1996 Jan 11; 61(2):158-63. PubMed ID: 8669444
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