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Journal Abstract Search

323 related items for PubMed ID: 9039997

  • 1. 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; 34(2):164-6. PubMed ID: 9039997
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  • 2. 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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  • 3. 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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  • 5. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
    Wieczorek D, Engels H, Viersbach R, Henke B, Schwanitz G, Passarge E.
    J Med Genet; 1998 Jul 15; 35(7):545-53. PubMed ID: 9678698
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  • 6. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O, Tastemir D.
    Fertil Steril; 2006 Jul 15; 86(1):219.e15-9. PubMed ID: 16818035
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  • 7. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z, Grebe TA, Guan XY, Notohamiprodjo M, Nutting PJ, Stone JF, Trent JM, Sandberg AA.
    Am J Med Genet; 1997 Aug 08; 71(2):160-6. PubMed ID: 9217215
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  • 8. 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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  • 9. 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 08; 88(4):482-3. PubMed ID: 1740326
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  • 10. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.
    Lockwood DH, Farrier A, Hecht F, Allanson J.
    Hum Genet; 1989 Oct 08; 83(3):287-8. PubMed ID: 2793173
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  • 11. 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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  • 14. Molecular cytogenetic characterization of a familial balanced reciprocal translocation t(11;18) (q13.3; q23) associated with pregnancy wastage.
    Liu JY, Wang XR, Zeng XL, Zhang CS, Hao S, Song YC.
    Cytogenet Genome Res; 2003 Dec 15; 103(1-2):8-13. PubMed ID: 15004456
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  • 15. 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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  • 16. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation.
    Hou JW.
    Chang Gung Med J; 2003 Jan 15; 26(1):48-52. PubMed ID: 12656309
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  • 17. 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 15; 18(4):233-8. PubMed ID: 7438504
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  • 18. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18.
    Lee MH, Park SY, Kim YM, Kim JM, Han JY, Kim MY, Ryu HM.
    Prenat Diagn; 2002 Feb 15; 22(2):102-4. PubMed ID: 11857612
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  • 19. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M, Przełozna B, Płodzien M, Bugno M, Wnuk M, Kotylak Z, Słota E.
    J Appl Genet; 2005 Feb 15; 46(4):419-21. PubMed ID: 16278518
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