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Journal Abstract Search

193 related items for PubMed ID: 11417485

  • 21. DNA polymorphism analysis in families with recurrence of free trisomy 21.
    Pangalos CG, Talbot CC, Lewis JG, Adelsberger PA, Petersen MB, Serre JL, Rethoré MO, de Blois MC, Parent P, Schinzel AA.
    Am J Hum Genet; 1992 Nov; 51(5):1015-27. PubMed ID: 1415248
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  • 22. Trisomic zygote rescue revealed by DNA polymorphism analysis in confined placental mosaicism.
    Sirchia SM, Garagiola I, Colucci G, Guerneri S, Lalatta F, Grimoldi MG, Simoni G.
    Prenat Diagn; 1998 Mar; 18(3):201-6. PubMed ID: 9556035
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  • 23. Origin of acrocentric trisomies in spontaneous abortuses.
    Niikawa N, Merotto E, Kajii T.
    Hum Genet; 1977 Dec 29; 40(1):73-8. PubMed ID: 604246
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  • 24. Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome.
    Kotzot D, Schinzel A.
    Eur J Hum Genet; 2000 Sep 29; 8(9):709-12. PubMed ID: 10980577
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  • 25. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.
    Robinson WP, Bernasconi F, Lau A, McFadden DE.
    Am J Med Genet; 1999 May 07; 84(1):34-42. PubMed ID: 10213044
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  • 26. Partial trisomy 1q, an uncommon chromosomal aberration in erythroleukemia.
    Baumgarten E, Wegner RD, Fengler R, Koch H, Henze G.
    Leuk Lymphoma; 1993 Jun 07; 10(3):237-40. PubMed ID: 8220123
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  • 27. Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events.
    Dahoun S, Gagos S, Gagnebin M, Gehrig C, Burgi C, Simon F, Vieux C, Extermann P, Lyle R, Morris MA, Antonarakis SE, Béna F, Blouin JL.
    Am J Med Genet A; 2008 Aug 15; 146A(16):2086-93. PubMed ID: 18627064
    [Abstract] [Full Text] [Related]

  • 28. Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.
    Kotzot D, Röthlisberger B, Riegel M, Schinzel A.
    J Med Genet; 2001 Dec 15; 38(12):876-81. PubMed ID: 11768394
    [No Abstract] [Full Text] [Related]

  • 29. Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.
    Ikonen RS, Lindlöf M, Janas MO, Simola KO, Millington-Ward A, de la Chapelle A.
    Hum Genet; 1989 Oct 15; 83(3):235-8. PubMed ID: 2571561
    [Abstract] [Full Text] [Related]

  • 30. Parental age and the origin of extra chromosome 21 in Down syndrome.
    Jyothy A, Kumar KS, Mallikarjuna GN, Babu Rao V, Uma Devi B, Sujatha M, Reddy PP.
    J Hum Genet; 2001 Oct 15; 46(6):347-50. PubMed ID: 11393539
    [Abstract] [Full Text] [Related]

  • 31. Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism.
    Perrin A, Douet-Guilbert N, Le Bris MJ, May-Panloup P, Guichet A, Amice V, Amice J, De Braekeleer M, Morel F.
    Int J Androl; 2009 Jun 15; 32(3):231-4. PubMed ID: 18217987
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  • 35. Incidence of mosaic cell lines in vivo and malsegregation of chromosome 21 in lymphocytes in vitro of trisomy 21 patients: detection by fluorescence in situ hybridization on binucleated lymphocytes.
    Shi Q, Adler ID, Zhang J, Zhang X, Shan X, Martin R.
    Hum Genet; 2000 Jan 15; 106(1):29-35. PubMed ID: 10982178
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  • 38. Mosaic trisomy 13: understanding origin using SNP array.
    Jinawath N, Zambrano R, Wohler E, Palmquist MK, Hoover-Fong J, Hamosh A, Batista DA.
    J Med Genet; 2011 May 15; 48(5):323-6. PubMed ID: 21097773
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  • 39. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM, Machado FB, Zampieri BL, Alves da Silva AF, Goloni-Bertollo EM, Haddad R, Eberlin MN, Vannucchi H, Carvalho VM, Medina-Acosta E, Pavarino-Bertelli EC.
    Genet Couns; 2009 May 15; 20(3):225-34. PubMed ID: 19852428
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