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Journal Abstract Search

67 related items for PubMed ID: 3137311

  • 1. [Genetic counseling in neurofibromatosis. Apropos of a study of 53 families].
    Toutain A, Kaplan J, Briard ML, Frézal J.
    J Genet Hum; 1988 Jun; 36(3):163-71. PubMed ID: 3137311
    [Abstract] [Full Text] [Related]

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

  • 3. Discounting an adverse maternal effect on severity of neurofibromatosis.
    Riccardi VM, Wald JS.
    Pediatrics; 1987 Mar; 79(3):386-93. PubMed ID: 3103092
    [Abstract] [Full Text] [Related]

  • 4. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 5. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
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  • 7. [Epidemiology of familial prostatic cancer: 4-year assessment of French studies].
    Valeri A, Drelon E, Azzouzi R, Delannoy A, Teillac P, Fournier G, Mangin P, Berthon P, Cussenot O.
    Prog Urol; 1999 Sep; 9(4):672-9. PubMed ID: 10555220
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  • 9. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.
    Terzi YK, Oguzkan-Balci S, Anlar B, Aysun S, Guran S, Ayter S.
    Genet Couns; 2009 Sep; 20(2):195-202. PubMed ID: 19650418
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  • 12. [Marfan disease].
    Briard ML, Chauvet ML, Kaplan J.
    J Genet Hum; 1988 Jun; 36(3):239-45. PubMed ID: 3411304
    [Abstract] [Full Text] [Related]

  • 13. [Variable expressiveness of behavior in patients with Recklinghausen's disease after genetic counseling].
    Manouvrier-Hanu S, Vandevelde-Staquet MF, Farriaux JP.
    J Genet Hum; 1988 Jun; 36(3):177-9. PubMed ID: 3137313
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  • 14. Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers.
    Oğuzkan S, Cinbiş M, Ayter S, Anlar B, Aysun S.
    Turk J Pediatr; 2003 Jun; 45(3):192-7. PubMed ID: 14696795
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  • 15. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].
    Marlin S, Denoyelle F, Garabédian EN, Petit C.
    Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):3-8. PubMed ID: 9765703
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  • 17. American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.
    American Society of Clinical Oncology.
    J Clin Oncol; 2003 Jun 15; 21(12):2397-406. PubMed ID: 12692171
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  • 18. Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic tool.
    Elyakim S, Lerer I, Zlotogora J, Sagi M, Gelman-Kohan Z, Merin S, Abeliovich D.
    Am J Med Genet; 1994 Dec 01; 53(4):325-34. PubMed ID: 7864041
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  • 20. [Treacher-Collins syndrome: clinical and genetic aspects apropos of 4 cases of which 1 is familial].
    Chaabouni M, Fersi M, Belghith N, Maazoul F, M'rad R, Ben Jemaa L, Gandoura N, Chaabouni H.
    Tunis Med; 2007 Oct 01; 85(10):885-90. PubMed ID: 18236814
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