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Journal Abstract Search

272 related items for PubMed ID: 4050866

  • 21. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM, Martin JA, Benjamin TR, Kukolich MK, Townsend-Parcham JK.
    Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
    [Abstract] [Full Text] [Related]

  • 22. Reciprocal translocations and full trisomy (trisomy 18 and trisomy 21) in the offspring.
    Fryns JP, Kleczkowska A, Moerman P, Van den Berghe H.
    Ann Genet; 1986; 29(4):272-4. PubMed ID: 3495232
    [Abstract] [Full Text] [Related]

  • 23. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990; 33(3):165-8. PubMed ID: 2288462
    [Abstract] [Full Text] [Related]

  • 24. Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism.
    Tunca Y, Wilroy RS, Kadandale JS, Martens PR, Gunther WM, Tharapel AT.
    Ann Genet; 2000; 43(1):39-43. PubMed ID: 10818220
    [Abstract] [Full Text] [Related]

  • 25. Partial 3p trisomy and different rearrangements involving chromosome 3 in the proposita's family.
    de Pina Neto JM, Ferrari I.
    Am J Med Genet; 1980; 5(1):25-33. PubMed ID: 7395898
    [Abstract] [Full Text] [Related]

  • 26. Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15).
    Stallings R, Vaughn D, Hall K, Joyce C, Ryan F, Barton D, Geraghty M.
    J Med Genet; 1997 Jun; 34(6):512-4. PubMed ID: 9192276
    [Abstract] [Full Text] [Related]

  • 27. [Partial trisomy 15q due to maternal translocation t(7;15)(q35;14)].
    Castel Y, Rivière D, Boycly JY, Toudic L.
    Ann Genet; 1976 Mar; 19(1):15-9. PubMed ID: 1084116
    [Abstract] [Full Text] [Related]

  • 28. Trisomy 14 mosaicism in a 5-year-old boy.
    Vachvanichsanong P, Jinorose U, Sangnuachua P.
    Am J Med Genet; 1991 Jul 01; 40(1):80-3. PubMed ID: 1887854
    [Abstract] [Full Text] [Related]

  • 29. Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24).
    Young SR, Donovan DM, Greer HA, Burch K, Potter DC.
    Hum Genet; 1976 Aug 30; 33(3):331-4. PubMed ID: 964994
    [Abstract] [Full Text] [Related]

  • 30. Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
    Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S.
    Genet Couns; 2004 Aug 30; 15(3):321-8. PubMed ID: 15517825
    [Abstract] [Full Text] [Related]

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  • 32. Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature.
    Léonard C, Huret JL, Imbert MC, Lebouc Y, Selva J, Boulley AM.
    Am J Med Genet; 1992 Jun 01; 43(3):621-5. PubMed ID: 1605261
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  • 34. Double aneuploidy: partial trisomy 21 and XO/XXX in a family with 12/21 translocation.
    Chen H, Tyrkus M, Woolley PV.
    Ann Genet; 1978 Sep 01; 21(3):177-80. PubMed ID: 315194
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  • 36. [Partial trisomy 12 and 8 with mosaicism, associated with translocation t(8;12) (p21;q13)].
    Savary JB, Cousin J, Laï JL, Deminatti M.
    Ann Genet; 1977 Jun 01; 20(2):122-7. PubMed ID: 302686
    [Abstract] [Full Text] [Related]

  • 37. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl.
    Jenkins EC, Curcuru-Giordano FM, Krishna SG, Cantarella J.
    Ann Genet; 1975 Jun 01; 18(2):117-20. PubMed ID: 1081364
    [Abstract] [Full Text] [Related]

  • 38. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.
    Fryns JP, Kleczkowska A, Decock P, Massa G, van den Berghe H.
    Ann Genet; 1992 Jun 01; 35(4):234-6. PubMed ID: 1296522
    [Abstract] [Full Text] [Related]

  • 39. Mosaic 5p tetrasomy.
    Stanley WS, Powell CM, Devine GC, Ellingham T, Samango-Sprouse CA, Vaught DR, Murphy BA, Rosenbaum KN.
    Am J Med Genet; 1993 Mar 15; 45(6):774-6. PubMed ID: 8456861
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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