BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]
    of 7.