These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

53 related articles for article (PubMed ID: 3557121)

  • 1. [Analysis of the diallelic model for the prevalence of epilepsy in families and populations].
    Ritsner MS; Drigalenko EI
    Genetika; 1987 Feb; 23(2):364-73. PubMed ID: 3557121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetico-epidemiologic analysis of the role of constitutional factors in the etiology of epilepsy].
    Ritsner MS
    Genetika; 1989 Feb; 25(2):372-80. PubMed ID: 2525506
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Estimate of the penetrance of genotypes in a monolocus model taking into account environmental factors].
    Drigalenko EI; Ritsner MS
    Genetika; 1987 May; 23(5):892-7. PubMed ID: 3623087
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS
    Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic liability to epilepsy in Kerala State, India.
    Nair RR; Thomas SV
    Epilepsy Res; 2004 Dec; 62(2-3):163-70. PubMed ID: 15579304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The parasite capacity of the host population].
    Kozminskiĭ EV
    Parazitologiia; 2002; 36(1):48-59. PubMed ID: 11965643
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Estimation of the parameters of the single-locus diallele model of qualitative trait in groups of relations].
    Drigalenko EI
    Genetika; 1985 Jun; 21(6):1034-8. PubMed ID: 4029611
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
    Marini C; Scheffer IE; Crossland KM; Grinton BE; Phillips FL; McMahon JM; Turner SJ; Dean JT; Kivity S; Mazarib A; Neufeld MY; Korczyn AD; Harkin LA; Dibbens LM; Wallace RH; Mulley JC; Berkovic SF
    Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [The use of the expectation-maximization (EM) algorithm for maximum likelihood estimation of gametic frequencies of multilocus polymorphic codominant systems based on sampled population data].
    Sergeev AS; Arapova RK
    Genetika; 2002 Mar; 38(3):407-18. PubMed ID: 11963570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The familial incidence of epilepsy in the group of epileptic patients examined after their first seizure--pilot study].
    Rózsavölgyi M; Rajna P
    Ideggyogy Sz; 2007 Jan; 60(1-2):23-9. PubMed ID: 17432090
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Comparative analysis of the proportion of genetic and environmental factors in the development of epilepsy].
    Ritsner MS; Karas' SI; Toĭtman LL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(6):810-3. PubMed ID: 6464597
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pseudo-likelihood estimates of the cumulative risk of an autosomal dominant disease from a kin-cohort study.
    Moore DF; Chatterjee N; Pee D; Gail MH
    Genet Epidemiol; 2001 Feb; 20(2):210-27. PubMed ID: 11180447
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Determination of the parameters of the single 2-allele autosomal locus model with incomplete penetrance].
    Finogenova SA
    Genetika; 1984 May; 20(5):841-8. PubMed ID: 6539726
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The resolution of genotype x environment interaction in segregation analysis of nuclear families.
    Eaves LJ
    Genet Epidemiol; 1984; 1(3):215-28. PubMed ID: 6544238
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inclusion of risk factor covariates in a segregation analysis of a population-based sample of 426 breast cancer families.
    Grabrick DM; Anderson VE; King RA; Kushi LH; Sellers TA
    Genet Epidemiol; 1999; 16(2):150-64. PubMed ID: 10030398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families.
    Winkelmann J; Muller-Myhsok B; Wittchen HU; Hock B; Prager M; Pfister H; Strohle A; Eisensehr I; Dichgans M; Gasser T; Trenkwalder C
    Ann Neurol; 2002 Sep; 52(3):297-302. PubMed ID: 12205641
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The heterogeneity problem. I: Separating genetic from environmental forms of the same disease.
    Greenberg DA; Hodge SE
    Am J Med Genet; 1985 Jun; 21(2):357-71. PubMed ID: 4014317
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High prevalence of epilepsy in a village in the Littoral Province of Cameroon.
    Prischich F; De Rinaldis M; Bruno F; Egeo G; Santori C; Zappaterreno A; Fattouch J; Di Bonaventura C; Bada J; Russo G; Pizzuti A; Cardona F; Sa'a ; Vullo V; Giallonardo AT; D'Erasmo E; Pelliccia A; Vanacore N
    Epilepsy Res; 2008 Dec; 82(2-3):200-10. PubMed ID: 18976884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Comparison of the multifactorial model as a hereditary mechanism of non-myoclonic generalized idiopathic epilepsy and partial idiopathic epilepsy].
    Sánchez JL; Jiménez I; Palacio LG; Jiménez M; Mora O; López-Gardner ; Zuluaga L; Uribe CS; Isaza R; Villa A; Blanco R; Arcos-Burgos M
    Rev Neurol; 1998 May; 26(153):739-44. PubMed ID: 9634657
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Segregation analysis of autosomal dominant polycystic kidney disease.
    Dobin A; Kimberling WJ; Pettinger W; Bailey-Wilson JE; Shugart YY; Gabow P
    Genet Epidemiol; 1993; 10(3):189-200. PubMed ID: 8349100
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.