BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 7717412)

  • 1. New heritable fragile site with spontaneous expression at 1q41.
    Dar H; Bar-El H; Ziv M; Shapiro I
    Am J Med Genet; 1995 Jan; 55(2):145-6. PubMed ID: 7717412
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 12q13 fragility in a family with recurrent spontaneous abortions: expression of the fragile site under different culture conditions.
    Giardino D; Bettio D; Simoni G
    Ann Genet; 1990; 33(2):88-91. PubMed ID: 2241090
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new heritable fragile site at 15q13 in a three-generation family.
    Zamani AG; Durakbasi-Dursun HG; Acar A
    Cytogenet Genome Res; 2007; 116(4):252-5. PubMed ID: 17431322
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Common fragile sites in couples with recurrent spontaneous abortions.
    Schlegelberger B; Gripp K; Grote W
    Am J Med Genet; 1989 Jan; 32(1):45-51. PubMed ID: 2495722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile site in chromosome 12 in a patient with two miscarriages.
    Stetten G; Sroka B; Norbury-Glaser M; Corson VL
    Am J Med Genet; 1988 Nov; 31(3):521-5. PubMed ID: 3228135
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new family with fra(10)(q25): spontaneous expression and 100% expression with 100 microM BrdU.
    Gollin SM; Bock HG; Caskey CT; Ledbetter DH
    Am J Med Genet; 1985 Aug; 21(4):643-8. PubMed ID: 4025395
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fragile sites and spontaneous abortions.
    Toncheva D
    Genet Couns; 1991; 2(4):205-10. PubMed ID: 1799417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 6p23 deletion mosaicism in a woman with recurrent abortions and idiopathic hypoprolactinemia.
    D'Alessandro E; Santiemma V; Lo Re ML; Ligas C; Del Porto G
    Am J Med Genet; 1992 Sep; 44(2):220-2. PubMed ID: 1456295
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression of folate sensitive and aphidicolin induced chromosomal fragile sites in familial neuroblastoma.
    Ankathil R; Kusumakumary P; Priyakumary T; Krishnan Nair M
    J Exp Clin Cancer Res; 2002 Sep; 21(3):383-8. PubMed ID: 12385582
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal fragile site at 2q13 in a proband with mental retardation.
    Kumada T; Kadotani T; Kanata S; Watanabe Y; Kurosaki N; Toi O
    Hiroshima J Med Sci; 1990 Mar; 39(1):19-21. PubMed ID: 2373639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A fragile site at 10q23 (FRA10A) in a phenytoin-exposed fetus: a case report and review of the literature.
    Morel CF; Duncan AM; Désilets V
    Prenat Diagn; 2005 Apr; 25(4):318-21. PubMed ID: 15849796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X).
    Daniel A; Ekblom L; Phillips S
    Am J Med Genet; 1984 Jul; 18(3):483-91. PubMed ID: 6476008
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New heritable fragile site at 15q13 in both members of a nonconsanguineous couple.
    Karadeniz NN; Tunca Y; Imirzalioğlu N
    Am J Med Genet A; 2003 Apr; 118A(3):290-2. PubMed ID: 12673662
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
    Wenger SL; Giangreco CA; Tarleton J; Wessel HB
    Am J Med Genet; 1996 Dec; 66(1):60-3. PubMed ID: 8957513
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new folate sensitive fragile site at 1p21.3.
    Baker E; Sutherland GR
    J Med Genet; 1991 May; 28(5):356-7. PubMed ID: 1865478
    [No Abstract]   [Full Text] [Related]  

  • 16. Bromodeoxyuridine induces chromosomal fragile sites in the canine genome.
    Stone DM; Stephens KE
    Am J Med Genet; 1993 Apr; 46(2):198-202. PubMed ID: 8484410
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unusual behaviour of a human autosome having two rare folate sensitive fragile sites.
    Sutherland GR; Baker E
    Ann Genet; 1993; 36(3):159-62. PubMed ID: 8117061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The determination of chromosome fragile sites in the peripheral blood lymphocytes of patients with colorectal cancer taking into account the cancer pathology predisposition in the familial anamnesis].
    Nesina IP; Polishchuk LZ; Oliĭnichenko PI
    Tsitol Genet; 2000; 34(1):3-9. PubMed ID: 10808535
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Heritable fragile sites on human chromosomes: characterization of a new BrdU-dependent site in 12q24].
    Croci G; Manenti E; Caselli L
    Pathologica; 1983; 75 Suppl():324-8. PubMed ID: 6680435
    [No Abstract]   [Full Text] [Related]  

  • 20. Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22.
    Stoll C; Roy-Doray B; Dott B; Alembik Y
    Genet Couns; 1997; 8(2):115-20. PubMed ID: 9219009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.