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Journal Abstract Search

164 related items for PubMed ID: 7450754

  • 21. Mosaic trisomy 9: two additional cases.
    Tropp MR, Currie M.
    Hum Genet; 1977 Sep 22; 38(2):131-5. PubMed ID: 908559
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  • 22. 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 22; 29(10):742-4. PubMed ID: 1433238
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  • 24. A female with XO/XY mosaicism and partial trisomy 9p.
    Klasen M, Hansmann I, Schmid M, Schmidtke J.
    J Med Genet; 1981 Dec 22; 18(6):482. PubMed ID: 7334513
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  • 28. Mapping of the gene for glutathione reductase on chromosome 8.
    de la Chapelle A, Icen A, Aula P, Leisti J, Turleau C, de Grouchy J.
    Ann Genet; 1976 Dec 22; 19(4):253-6. PubMed ID: 1087855
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  • 29. Trisomy 8 in the bone marrow associated with high red cell glutathione reductase activity.
    de la Chapelle A, Vuopio P, Icén A.
    Blood; 1976 May 22; 47(5):815-26. PubMed ID: 1063047
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  • 30. Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.
    Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.
    Pediatr Dermatol; 2004 May 22; 21(6):636-41. PubMed ID: 15575846
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  • 31. Trisomy 12 mosaicism in an infertile man.
    Richer CL, Bleau G, Chapdelaine A.
    Can J Genet Cytol; 1977 Sep 22; 19(3):565-7. PubMed ID: 589516
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  • 32. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J.
    Ann Genet; 1979 Sep 22; 22(3):178-81. PubMed ID: 316677
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  • 33. [Mosaic trisomy of chromosome 20 in a patient with congenital anomalies--10-years observation].
    Barg E, Gil J, Wikiera B, Smigiel R.
    Pediatr Endocrinol Diabetes Metab; 2009 Sep 22; 15(4):266-70. PubMed ID: 20455422
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  • 34. Secondary trisomy or mosaic "tetrasomy" 8p.
    Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.
    Am J Med Genet; 1989 Mar 22; 32(3):320-4. PubMed ID: 2729351
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  • 35. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
    Voss R, Gross-Kieselstein E, Hurvitz H, Dagan J, Kerem E, Zlotogora J.
    J Med Genet; 1984 Dec 22; 21(6):454-9. PubMed ID: 6512835
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  • 37. Pigmentary dysplasias in long survivors with mosaic trisomy 18: report of two cases.
    Murano I, Ohashi H, Tsukahara M, Tonoki H, Okino F, Atsumi M, Kajii T.
    Clin Genet; 1991 Jan 22; 39(1):68-74. PubMed ID: 1997220
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  • 38. Duplication of the short arm of chromosome 9. Analysis of five cases.
    Cuoco C, Gimelli G, Pasquali F, Poloni L, Zuffardi O, Alicata P, Battaglino G, Bernardi F, Cerone R, Cotellessa M, Ghidoni A, Motta S.
    Hum Genet; 1982 Jan 22; 61(1):3-7. PubMed ID: 7129421
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  • 39. Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9.
    Frydman M, Shabtal F, Halbrecht I, Elian E.
    J Med Genet; 1981 Oct 22; 18(5):390-2. PubMed ID: 7328619
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  • 40. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH, Broske SP, Moore CM, Thomas GH, Neill CA.
    J Med Genet; 1973 Jun 22; 10(2):180-4. PubMed ID: 4714587
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