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Journal Abstract Search

67 related items for PubMed ID: 3137311

  • 21. Sex ratio distortion in offspring of families with BRCA1 or BRCA2 mutant alleles: an ascertainment bias phenomenon?
    Balmaña J, Díez O, Campos B, Majewski M, Sanz J, Alonso C, Baiget M, Garber JE.
    Breast Cancer Res Treat; 2005 Aug; 92(3):273-7. PubMed ID: 16155798
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  • 23. The association between parental bonding and obsessive compulsive disorder in offspring at high familial risk.
    Wilcox HC, Grados M, Samuels J, Riddle MA, Bienvenu OJ, Pinto A, Cullen B, Wang Y, Shugart YY, Liang KY, Nestadt G.
    J Affect Disord; 2008 Nov; 111(1):31-9. PubMed ID: 18299151
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  • 24. Clinical application of genetic polymorphism in neurofibromatosis type 1.
    Clementi M, Boni S, Mammi I, Favarato M, Tenconi R.
    Ann Genet; 1996 Nov; 39(2):92-6. PubMed ID: 8766140
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  • 27. Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics.
    Aalfs CM, Mollema ED, Oort FJ, de Haes JC, Leschot NJ, Smets EM.
    Clin Genet; 2004 Aug; 66(2):112-21. PubMed ID: 15253761
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  • 28. [Huntington's disease. Contribution of clinical and epidemiological data to genetic counseling].
    Petit H, Salomez JL.
    J Genet Hum; 1985 Jun; 33(2):91-102. PubMed ID: 3160829
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  • 31. Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.
    Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J.
    Am J Gastroenterol; 2002 Dec; 97(12):3095-101. PubMed ID: 12492195
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  • 32. Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA.
    de Raedt T, Cools J, Debiec-Rychter M, Brems H, Mentens N, Sciot R, Himpens J, de Wever I, Schöffski P, Marynen P, Legius E.
    Gastroenterology; 2006 Dec; 131(6):1907-12. PubMed ID: 17087943
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  • 33. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.
    Brito D, Richard P, Komajda M, Madeira H.
    Rev Port Cardiol; 2008 Feb; 27(2):147-73. PubMed ID: 18488914
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  • 36. Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2).
    Zhao Y, Kumar RA, Baser ME, Evans DG, Wallace A, Kluwe L, Mautner VF, Parry DM, Rouleau GA, Joe H, Friedman JM.
    Genet Epidemiol; 2002 Oct; 23(3):245-59. PubMed ID: 12384977
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  • 39. [Active screening for genetic pathology in newborns. II. Genetic counseling and prenatal diagnosis in high risk families].
    Kovacheva K, Angelova L, Simeonova M.
    Akush Ginekol (Sofiia); 2004 Oct; 43(5):32-5. PubMed ID: 15518282
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