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Journal Abstract Search

74 related items for PubMed ID: 7198599

  • 1. [Table method of component partition of phenotypic dispersion for identifying the X chromosome effect based on correlations between relatives].
    Trubnikov VI, Ageev SV, Gindilis VM.
    Genetika; 1981; 17(11):2034-43. PubMed ID: 7198599
    [Abstract] [Full Text] [Related]

  • 2. [Table method of the component expansion of phenotypic variance based on correlations between relatives].
    Trubnikov VI, Gindilis VM.
    Genetika; 1981; 17(6):1107-16. PubMed ID: 7019005
    [Abstract] [Full Text] [Related]

  • 3. [Identification of the effects of the X chromosome in component partitioning of phenotypic variance].
    Ageev SV.
    Genetika; 1982 Jul; 18(7):1149-60. PubMed ID: 6889551
    [Abstract] [Full Text] [Related]

  • 4. [Algorithm for calculating the probabilities of the identity of genes by descent in arbitrary pedigrees].
    Ageev SV.
    Genetika; 1983 Apr; 19(4):670-8. PubMed ID: 6683213
    [Abstract] [Full Text] [Related]

  • 5. Sex differences in genetic and environmental determinants of pulse pressure.
    Scurrah KJ, Byrnes GB, Hopper JL, Harrap SB.
    Genet Epidemiol; 2006 Jul; 30(5):397-408. PubMed ID: 16732554
    [Abstract] [Full Text] [Related]

  • 6. The correlation between relatives under assortative malting for an X-linked and autosomal trait.
    Risch H.
    Ann Hum Genet; 1979 Oct; 43(2):151-65. PubMed ID: 525974
    [Abstract] [Full Text] [Related]

  • 7. Multipoint linkage analysis of quantitative traits on sex-chromosomes.
    Ekstrøm CT.
    Genet Epidemiol; 2004 Apr; 26(3):218-30. PubMed ID: 15022208
    [Abstract] [Full Text] [Related]

  • 8. Power of variance component linkage analysis to detect epistasis.
    Mitchell BD, Ghosh S, Schneider JL, Birznieks G, Blangero J.
    Genet Epidemiol; 1997 Apr; 14(6):1017-22. PubMed ID: 9433617
    [Abstract] [Full Text] [Related]

  • 9. The mechanism of emergenesis.
    Lykken DT.
    Genes Brain Behav; 2006 Jun; 5(4):306-10. PubMed ID: 16716200
    [Abstract] [Full Text] [Related]

  • 10. Two-locus drift with sex chromosomes: the partitioning and conversion of variance in subdivided populations.
    Whitlock MC.
    Theor Popul Biol; 1995 Aug; 48(1):44-64. PubMed ID: 7660328
    [Abstract] [Full Text] [Related]

  • 11. Familial correlational analyses, sex differences, and the X-linked gene hypothesis.
    Thomas H.
    Psychol Bull; 1983 May; 93(3):427-40. PubMed ID: 6346370
    [No Abstract] [Full Text] [Related]

  • 12. Genetic factors in cephalo facial measurements at birth as revealed by new born-parent correlations.
    Murty JS, Annapurna V.
    Acta Anthropogenet; 1982 May; 6(2):107-14. PubMed ID: 7171391
    [Abstract] [Full Text] [Related]

  • 13. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY.
    Am J Med Genet; 1994 Nov 01; 53(2):108-40. PubMed ID: 7856637
    [Abstract] [Full Text] [Related]

  • 14. The estimation of maternal genetic variances.
    Thompson R.
    Biometrics; 1976 Dec 01; 32(4):903-17. PubMed ID: 1009230
    [Abstract] [Full Text] [Related]

  • 15. Monochorionic-diamniotic twins discordant in gender from a naturally conceived pregnancy through postzygotic sex chromosome loss in a 47,XXY zygote.
    Zech NH, Wisser J, Natalucci G, Riegel M, Baumer A, Schinzel A.
    Prenat Diagn; 2008 Aug 01; 28(8):759-63. PubMed ID: 18567067
    [Abstract] [Full Text] [Related]

  • 16. Heritability and heteromorphic distributions of AluI chromosome banding variants in twins.
    Huang B, Meyer JM, Jackson-Cook CK.
    Am J Med Genet; 1995 Jul 03; 57(3):429-36. PubMed ID: 7677146
    [Abstract] [Full Text] [Related]

  • 17. Genome screen for a combined bone phenotype using principal component analysis: the Framingham study.
    Karasik D, Cupples LA, Hannan MT, Kiel DP.
    Bone; 2004 Mar 03; 34(3):547-56. PubMed ID: 15003802
    [Abstract] [Full Text] [Related]

  • 18. How stable are personality traits?
    Eaves LJ, Young PA.
    Prog Clin Biol Res; 1981 Mar 03; 69 Pt B():87-97. PubMed ID: 7199179
    [No Abstract] [Full Text] [Related]

  • 19. Frontometaphyseal dysplasia--evidence for X-linked inheritance.
    Gorlin RJ, Winter RB.
    Am J Med Genet; 1980 Mar 03; 5(1):81-4. PubMed ID: 7395904
    [Abstract] [Full Text] [Related]

  • 20. Twin pregnancy in woman with 45,X/47,XXX karyotype.
    Kivinen S, Herva R.
    Obstet Gynecol; 1980 Sep 03; 56(3):401-2. PubMed ID: 7422184
    [Abstract] [Full Text] [Related]

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