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]