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Journal Abstract Search

379 related items for PubMed ID: 8741873

  • 41. Variable clinical expression of mosaic trisomy 16 in the newborn infant.
    Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P.
    Am J Med Genet; 1993 Aug 15; 47(2):294-8. PubMed ID: 8213923
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  • 42. Amniotic trisomy 11 mosaicism--is it a benign finding?
    Basel-Vanagaite L, Davidov B, Friedman J, Yeshaya Y, Magal N, Drasinover V, Shohat M.
    Prenat Diagn; 2006 Sep 15; 26(9):778-81. PubMed ID: 16810710
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  • 47. Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.
    L'Herminé AC, Aboura A, Brisset S, Cuisset L, Castaigne V, Labrune P, Frydman R, Tachdjian G.
    Prenat Diagn; 2003 Nov 15; 23(11):938-43. PubMed ID: 14634983
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  • 48. Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.
    Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD.
    Am J Med Genet; 1996 Nov 11; 65(4):348-52. PubMed ID: 8923948
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  • 49. Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16.
    Schneider AS, Bischoff FZ, McCaskill C, Coady ML, Stopfer JE, Shaffer LG.
    Am J Med Genet; 1996 Dec 11; 66(2):204-8. PubMed ID: 8958332
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  • 51. Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
    Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H.
    Prenat Diagn; 2000 Feb 11; 20(2):103-22. PubMed ID: 10694683
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  • 52. Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellum.
    Abdelhedi F, El Khattabi L, Cuisset L, Tsatsaris V, Viot G, Druart L, Lebbar A, Dupont JM.
    Am J Clin Pathol; 2014 Aug 11; 142(2):248-53. PubMed ID: 25015868
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  • 53. Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin.
    Paulyson KJ, Sherer DM, Christian SL, Lewis KM, Ledbetter DH, Salafia CM, Meck JM.
    Prenat Diagn; 1996 Nov 11; 16(11):1021-6. PubMed ID: 8953635
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  • 54. A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.
    Ushijima K, Yatsuga S, Matsumoto T, Nakamura A, Fukami M, Kagami M.
    J Hum Genet; 2018 Mar 11; 63(3):377-381. PubMed ID: 29311684
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  • 57. Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20.
    Salafsky IS, MacGregor SN, Claussen U, von Eggeling F.
    Prenat Diagn; 2001 Oct 11; 21(10):860-3. PubMed ID: 11746130
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  • 59. Prenatally detected trisomy 20 mosaicism.
    Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK.
    Prenat Diagn; 2005 Mar 11; 25(3):239-44. PubMed ID: 15791659
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  • 60. The maternal uniparental disomy of chromosome 6 (upd(6)mat) "phenotype": result of placental trisomy 6 mosaicism?
    Eggermann T, Oehl-Jaschkowitz B, Dicks S, Thomas W, Kanber D, Albrecht B, Begemann M, Kurth I, Beygo J, Buiting K.
    Mol Genet Genomic Med; 2017 Nov 11; 5(6):668-677. PubMed ID: 29178649
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