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PUBMED FOR HANDHELDS

Journal Abstract Search


124 related items for PubMed ID: 9237504

  • 21. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.
    Schrander-Stumpel C, Schrander J, Fryns JP, Hamers G.
    Clin Genet; 1990 Feb; 37(2):148-52. PubMed ID: 2178819
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  • 25. Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones.
    Miller K, Arslan-Kirchner A, Schulze B, Dudel-Neujahr A, Morlot M, Burck U, Gerresheim F.
    Ann Genet; 1997 Feb; 40(3):181-4. PubMed ID: 9401109
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  • 26. An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
    Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF.
    Eur J Pediatr; 2008 Jun; 167(6):655-9. PubMed ID: 17668239
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  • 27. A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.
    Willatt LR, Davison BC, Goudie D, Alexander J, Dyson HM, Jenks PE, Ferguson-Smith ME.
    J Med Genet; 1992 Oct; 29(10):742-4. PubMed ID: 1433238
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  • 30. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH, Broske SP, Moore CM, Thomas GH, Neill CA.
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
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  • 31. Prenatal diagnosis of mosaicism for triploidy and trisomy 13.
    Phelan MC, Curtis Rogers R, Michaelis RC, Moore CL, Blackburn W.
    Prenat Diagn; 2001 Jun; 21(6):457-60. PubMed ID: 11438949
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  • 32. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC).
    Prenat Diagn; 1999 Jan; 19(1):29-35. PubMed ID: 10073903
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  • 33. A three-year follow-up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally.
    Camurri L, Chiesi A.
    Prenat Diagn; 1991 Jan; 11(1):59-62. PubMed ID: 2027856
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  • 34. Complete and partial trisomy of different segments of chromosome 8: case reports and review.
    Fineman RM, Ablow RC, Breg WR, Wing SD, Rose JS, Rothman SL, Warpinski J.
    Clin Genet; 1979 Dec; 16(6):390-8. PubMed ID: 527246
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  • 37. The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues.
    Papavassiliou P, York TP, Gursoy N, Hill G, Nicely LV, Sundaram U, McClain A, Aggen SH, Eaves L, Riley B, Jackson-Cook C.
    Am J Med Genet A; 2009 Feb 15; 149A(4):573-83. PubMed ID: 19291777
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