125 related articles for article (PubMed ID: 15389713)
21. Familial translocation 15-22. A possible cause for abortions in female carriers.
Fried K; Bukovsky J; Rosenblatt M; Mundel G
J Med Genet; 1974 Sep; 11(3):280-2. PubMed ID: 4431033
[TBL] [Abstract][Full Text] [Related]
22. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
Bacino CA; Kashork CD; Davino NA; Shaffer LG
Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
[TBL] [Abstract][Full Text] [Related]
23. Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier.
Pellestor F; Puechberty J; Weise A; Lefort G; Anahory T; Liehr T; Sarda P
Fertil Steril; 2011 Jun; 95(7):2433.e17-22. PubMed ID: 21367411
[TBL] [Abstract][Full Text] [Related]
24. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
Shaffer LG; Spikes AS; Macha M; Dunn R
J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
[TBL] [Abstract][Full Text] [Related]
25. Recurrent miscarriage in a carrier of a balanced cytogenetically undetectable subtelomeric rearrangement: how many are we missing?
Alkuraya FS; Martin CL; Kimonis VE
Prenat Diagn; 2006 Mar; 26(3):291-3. PubMed ID: 16506278
[No Abstract] [Full Text] [Related]
26. Reciprocal translocation with special reference to reproductive failure.
Subrt I
Hum Genet; 1980; 55(3):303-7. PubMed ID: 7203462
[TBL] [Abstract][Full Text] [Related]
27. De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter.
Timár L; Béres J; Kosztolányi G; Németh I
Hum Genet; 1991 Feb; 86(4):421. PubMed ID: 1999348
[TBL] [Abstract][Full Text] [Related]
28. Trisomy 20p from maternal translocation and anencephaly. Case report and genetic review.
Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López Pajares I
Ann Genet; 1989; 32(4):247-9. PubMed ID: 2610493
[TBL] [Abstract][Full Text] [Related]
29. Familial C/D translocation t(9;13)(9p23.13q21) in a male associated with recurrent abortion.
Singh-Kahlon D; Serra A
Hum Genet; 1976 Aug; 33(3):223-30. PubMed ID: 964984
[TBL] [Abstract][Full Text] [Related]
30. Familial paracentric inversions inv(2)(q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities.
Lin CC; Bowen P; Hoo JJ
Hum Genet; 1987 Jan; 75(1):84-7. PubMed ID: 3804335
[TBL] [Abstract][Full Text] [Related]
31. Familial occurrence of chromosome 7/12 translocation.
Ming PM; Parker R; Goodner DM
Clin Genet; 1980 Dec; 18(6):445-9. PubMed ID: 7449184
[TBL] [Abstract][Full Text] [Related]
32. An unusual translocation 46,XX,t(14;17)(q33.2;p11.2) in a woman with recurrent spontaneous abortions.
Calzolari E; Azzini G; Palazzi P; Raffaella Contiero M
Hum Genet; 1985; 71(2):181. PubMed ID: 4043969
[No Abstract] [Full Text] [Related]
33. Chromosomal abnormalities in couples with recurrent abortions.
Low PS; Tay JS; Tan MA; Chua TS; Wong HB
J Singapore Paediatr Soc; 1989; 31(1-2):72-4. PubMed ID: 2770260
[TBL] [Abstract][Full Text] [Related]
34. Homologous Robertsonian translocation (21q21q) and abortions.
Sudha T; Gopinath PM
Hum Genet; 1990 Jul; 85(2):253-5. PubMed ID: 2142474
[TBL] [Abstract][Full Text] [Related]
35. Detection of a familial cryptic translocation by fluorescent in situ hybridisation.
Smith DP; Floyd M; Say B
J Med Genet; 1996 Jan; 33(1):84. PubMed ID: 8825058
[No Abstract] [Full Text] [Related]
36. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
Liehr T; Heller A; Eichhorn KH; Beensen V; Schulze E; Starke H; Claussen U; Schreyer I
Prenat Diagn; 2004 Dec; 24(12):1022-4. PubMed ID: 15614895
[No Abstract] [Full Text] [Related]
37. 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]
38. [Double translocation 46, XX, t(2; 5), t(2; 18) with major reproduction problems].
Sidaner I; Nivelon-Chevallier A; Mugneret F; Turc-Carel C
J Genet Hum; 1988 Jan; 36(1-2):89-92. PubMed ID: 3379383
[TBL] [Abstract][Full Text] [Related]
39. [Chromosome 6/17 translocation as a cause of repeated abortions].
Pasquali F; Maraschio P; Zara C
Ann Ostet Ginecol Med Perinat; 1973; 94(9-10):553-9. PubMed ID: 4806141
[No Abstract] [Full Text] [Related]
40. Translocation (14;21)(q11;q22) in a woman with history of abortions and a child with Down's syndrome.
Sudha T; Gopinath PM
Ann Genet; 1990; 33(3):162-4. PubMed ID: 2149630
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]