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Journal Abstract Search

145 related items for PubMed ID: 589852

  • 21. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
    Tranebjaerg L, Baekmark UB, Dyhr-Nielsen M, Kreiborg S.
    Clin Genet; 1987 Aug; 32(2):137-43. PubMed ID: 3652493
    [Abstract] [Full Text] [Related]

  • 22. Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10.
    Herva R, Korhonen S, Haapala K, Timonen E.
    Clin Genet; 1983 Jul; 24(1):50-3. PubMed ID: 6616946
    [Abstract] [Full Text] [Related]

  • 23. Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10q.
    Larson LM, Wasdahl WA, Saumur JH, Coleman ML, Hall JG, Dolan CR, Schutta CJ.
    Clin Genet; 1982 Mar; 21(3):187-95. PubMed ID: 7094394
    [Abstract] [Full Text] [Related]

  • 24. [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].
    Laurent C, Bovier-Lapierre M, Dutrillaux B.
    Humangenetik; 1973 Mar; 18(4):321-7. PubMed ID: 4200006
    [No Abstract] [Full Text] [Related]

  • 25. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
    Coco R, del Rey G.
    J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
    [Abstract] [Full Text] [Related]

  • 26. Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I.
    Petković I, de Capoa A, Giancotti P, Barisić I.
    Clin Genet; 1996 Dec; 50(6):515-9. PubMed ID: 9147886
    [Abstract] [Full Text] [Related]

  • 27. A familial F/G translocation [t(p-; 22q+)] observed in three generations.
    Cohen MM, Davidson RG, Brown JA.
    Clin Genet; 1975 Feb; 7(2):120-7. PubMed ID: 1132159
    [Abstract] [Full Text] [Related]

  • 28. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11).
    Carnevale A, Frías S, del Castillo V.
    Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358
    [Abstract] [Full Text] [Related]

  • 29. Segregation of two independent chromosomal translocations in one family.
    Miller K, Flatz SD.
    Hum Genet; 1984 Oct; 68(1):93-5. PubMed ID: 6500562
    [Abstract] [Full Text] [Related]

  • 30. Tertiary trisomy 14q--, due to paternal balanced translocation 46,XY,t(1;14)(q44;q22).
    Kovacs G, Mihai C.
    Hum Genet; 1979 Jun 19; 49(2):175-8. PubMed ID: 468247
    [Abstract] [Full Text] [Related]

  • 31. Trisomy 13 with a 13q14q translocation.
    Coco R, Penchaszadeh B.
    J Genet Hum; 1975 Mar 19; 23(1):1-6. PubMed ID: 1165477
    [Abstract] [Full Text] [Related]

  • 32. Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.
    Simpson J, Zellweger H.
    J Med Genet; 1977 Apr 19; 14(2):124-7. PubMed ID: 853318
    [Abstract] [Full Text] [Related]

  • 33. Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation.
    Armendares S, Salamanca-Gómez F.
    Clin Genet; 1978 Jan 19; 13(1):17-24. PubMed ID: 624187
    [Abstract] [Full Text] [Related]

  • 34. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment.
    Cohen MM, Lerner C, Balkin NE.
    Am J Med Genet; 1983 Jan 19; 14(1):89-96. PubMed ID: 6829613
    [Abstract] [Full Text] [Related]

  • 35. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984 Jan 19; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 36. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE, Kooper AJ, Winarni TI, Smits AP, Faradz SM, Hamel BC.
    Genet Couns; 2010 Jan 19; 21(1):99-108. PubMed ID: 20420036
    [Abstract] [Full Text] [Related]

  • 37. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M, Wethling H, Niemeyer ML, Schwinger E.
    Klin Padiatr; 1987 Jan 19; 199(1):27-31. PubMed ID: 2435950
    [Abstract] [Full Text] [Related]

  • 38. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD, Pitmon D, Schorderet D, Engel E.
    J Genet Hum; 1985 Dec 19; 33(5):371-80. PubMed ID: 4093767
    [Abstract] [Full Text] [Related]

  • 39. [Partial 4q trisomy. Apropos of 3 cases].
    Dutrillaux B, Laurent C, Forabosco A, Noel B, Suerinc E, Biemont MC, Cotton JB.
    Ann Genet; 1975 Mar 19; 18(1):21-7. PubMed ID: 238457
    [Abstract] [Full Text] [Related]

  • 40.
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