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Journal Abstract Search

498 related items for PubMed ID: 4130026

  • 1. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.
    Kakati S, Sinha AK.
    Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026
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  • 6. A familial Y-autosome translocation in man.
    Noel B, Emerit I, Luciani JM, Quack B.
    Clin Genet; 1971 Apr; 2(1):1-6. PubMed ID: 5111751
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  • 10. X-autosome translocation in normal mother and effectively 21-monosomic daughter.
    Summitt RL, Martens PR, Wilroy RS.
    J Pediatr; 1974 Apr; 84(4):539-46. PubMed ID: 4834247
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  • 12. Letter: Brilliantly fluorescing enlarged short arms D or G.
    Nielsen J, Friedrich U, Hreidarsson AB, Noel B, Quack B, Mottet J.
    Lancet; 1974 May 25; 1(7865):1049-50. PubMed ID: 4133722
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  • 13. [Cytogenetic studies of families of patients with Down's syndrome].
    Davidenkova EF, Kolosova NN, Pantova IG, Shushval ON.
    Tsitologiia; 1966 May 25; 8(2):277-82. PubMed ID: 4228480
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  • 14. Quantitative studies of Y chromosomal fluorescence in human interphase nuclei.
    Lamborot-Manzur M, Tishler PV, Atkins L.
    Clin Genet; 1972 May 25; 3(2):103-15. PubMed ID: 4115478
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  • 15. Familial cases of marker chromosomes of groups 21-22 and 13-15 (Gpss and Dp+).
    Kyaosaar ME.
    Sov Genet; 1973 Nov 15; 7(7):913-8. PubMed ID: 4777944
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  • 18. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.
    Hamerton JL, Canning N, Ray M, Smith S.
    Clin Genet; 1975 Oct 15; 8(4):223-43. PubMed ID: 1183067
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  • 19. Structural variation in human nitotic chromosomes.
    Leisti J.
    Ann Acad Sci Fenn Biol; 1971 Oct 15; 179():1-69. PubMed ID: 4261167
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