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Journal Abstract Search

383 related items for PubMed ID: 8950677

  • 1. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22.
    Dawson AJ, Mears AJ, Chudley AE, Bech-Hansen T, McDermid H.
    J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677
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  • 2. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW.
    Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309
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  • 3. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
    Zackai EH, Emanuel BS.
    Am J Med Genet; 1980 Jan; 7(4):507-21. PubMed ID: 7211960
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  • 4. Emanuel syndrome due to unusual segregation of paternal origin.
    Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO.
    Genet Couns; 2012 Jan; 23(2):319-28. PubMed ID: 22876593
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  • 5. Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.
    Petković I, de Capoa A, Giancotti P, Barisić I.
    Clin Genet; 1996 Dec; 50(6):515-9. PubMed ID: 9147886
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  • 8. A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature.
    Paththinige CS, Sirisena ND, Kariyawasam UGIU, Ediriweera RC, Kruszka P, Muenke M, Dissanayake VHW.
    BMC Med Genomics; 2018 May 08; 11(1):44. PubMed ID: 29739404
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  • 9. Meiotic chromosome segregation in human t(11;22)(q23;q11) carriers: a theoretical consideration.
    Koduru PR, Chaganti RS.
    Genome; 1989 Feb 08; 32(1):24-9. PubMed ID: 2721946
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  • 11. Familial complex chromosome rearrangement ascertained by in situ hybridisation.
    Fuster C, Miguez L, Miró R, Rigola MA, Perez A, Egozcue J.
    J Med Genet; 1997 Feb 08; 34(2):164-6. PubMed ID: 9039997
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  • 12. Unbalanced karyotype due to adjacent 1 segregation of t(11;22)(q23.3;q13.2).
    Tachdjian G, Muti C, Gaudelus J, Druart L, Martin B, Tamboise E, Nessmann C.
    Ann Genet; 1992 Feb 08; 35(4):231-3. PubMed ID: 1296521
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  • 13. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
    Armstrong SJ, Goldman AS, Speed RM, Hultén MA.
    Am J Hum Genet; 2000 Sep 08; 67(3):601-9. PubMed ID: 10936106
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  • 14. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
    Kulharya AS, Lovell CM, Flannery DB.
    Am J Med Genet; 2002 Dec 15; 113(4):367-70. PubMed ID: 12457409
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  • 16. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK, Wilroy RS, Summitt JB, Tucker B, Herrod HG, Tharapel AT.
    Am J Med Genet; 1990 Sep 15; 37(1):92-6. PubMed ID: 2240050
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  • 17. 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 15; 104(5):412-7. PubMed ID: 10394934
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  • 18. Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation.
    Zimmermann-Bär U, Stallmach T, Riegel M, Wiedemann U, Fauchère JC, Binkert F, Kotzot D.
    Prenat Diagn; 2000 Oct 15; 20(10):847-50. PubMed ID: 11038468
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  • 19. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Oct 15; 23(2):239-47. PubMed ID: 22876583
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  • 20. 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 15; 25(8):683-6. PubMed ID: 16049998
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