These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 3478296)

  • 21. A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.
    Tanzi RE; Watkins PC; Stewart GD; Wexler NS; Gusella JF; Haines JL
    Am J Hum Genet; 1992 Mar; 50(3):551-8. PubMed ID: 1347193
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Association between maternal age and meiotic recombination for trisomy 21.
    Lamb NE; Yu K; Shaffer J; Feingold E; Sherman SL
    Am J Hum Genet; 2005 Jan; 76(1):91-9. PubMed ID: 15551222
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Origin and mechanisms of non-disjunction in human autosomal trisomies.
    Nicolaidis P; Petersen MB
    Hum Reprod; 1998 Feb; 13(2):313-9. PubMed ID: 9557829
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.
    Eggermann T; Nöthen MM; Eiben B; Hofmann D; Hinkel K; Fimmers R; Schwanitz G
    Hum Genet; 1996 Feb; 97(2):218-23. PubMed ID: 8566957
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A revised map of chromosome 1.
    Sherman SL; King J; Robson EB; Yee S
    Ann Hum Genet; 1984 Jul; 48(3):243-51. PubMed ID: 6589974
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosomal differences in susceptibility to meiotic aneuploidy.
    Warburton D; Kinney A
    Environ Mol Mutagen; 1996; 28(3):237-47. PubMed ID: 8908182
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Likelihood of a particular order of genetic markers and the construction of genetic maps.
    Tewari S; Arnold J; Bhandarkar SM
    J Bioinform Comput Biol; 2008 Feb; 6(1):125-62. PubMed ID: 18324750
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions.
    Göring HH; Terwilliger JD
    Am J Hum Genet; 2000 Mar; 66(3):1107-18. PubMed ID: 10712221
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Recombination across the centromere of disjoined and non-disjoined chromosome 21.
    Laurent AM; Li M; Sherman S; Roizès G; Buard J
    Hum Mol Genet; 2003 Sep; 12(17):2229-39. PubMed ID: 12915463
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytogenetic and molecular studies of trisomy 13.
    Hassold T; Jacobs PA; Leppert M; Sheldon M
    J Med Genet; 1987 Dec; 24(12):725-32. PubMed ID: 2892938
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multilocus analysis for gene-centromere mapping using first polar bodies and secondary oocytes.
    Da Y; Jarrell VL; Wang T; Fernando RL; Wheeler MB; Lewin HA
    Genetics; 1995 Feb; 139(2):1091-7. PubMed ID: 7713411
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Bias of the estimated recombination fraction and lod score due to an association between a disease gene and a marker gene.
    Clerget-Darpoux F
    Ann Hum Genet; 1982 Oct; 46(4):363-72. PubMed ID: 6961885
    [No Abstract]   [Full Text] [Related]  

  • 33. Nondisjunction in trisomy 21: origin and mechanisms.
    Petersen MB; Mikkelsen M
    Cytogenet Cell Genet; 2000; 91(1-4):199-203. PubMed ID: 11173856
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
    Lamb NE; Feingold E; Savage A; Avramopoulos D; Freeman S; Gu Y; Hallberg A; Hersey J; Karadima G; Pettay D; Saker D; Shen J; Taft L; Mikkelsen M; Petersen MB; Hassold T; Sherman SL
    Hum Mol Genet; 1997 Sep; 6(9):1391-9. PubMed ID: 9285774
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.
    Thomas NS; Ennis S; Sharp AJ; Durkie M; Hassold TJ; Collins AR; Jacobs PA
    Hum Mol Genet; 2001 Feb; 10(3):243-50. PubMed ID: 11159943
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Analysis of crossingover in man.
    Morton NE
    Cytogenet Cell Genet; 1978; 22(1-6):15-36. PubMed ID: 752468
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping.
    Meijer H; Hamers GJ; Jongbloed RJ; Vaes-Peeters GP; van der Hulst RR; Geraedts JP
    Hum Genet; 1989 Oct; 83(3):280-6. PubMed ID: 2571564
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Computational Approach to Estimating Nondisjunction Frequency in Saccharomyces cerevisiae.
    Chu DB; Burgess SM
    G3 (Bethesda); 2016 Jan; 6(3):669-82. PubMed ID: 26747203
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
    Karadima G; Bugge M; Nicolaidis P; Vassilopoulos D; Avramopoulos D; Grigoriadou M; Albrecht B; Passarge E; Annerén G; Blennow E; Clausen N; Galla-Voumvouraki A; Tsezou A; Kitsiou-Tzeli S; Hahnemann JM; Hertz JM; Houge G; Kuklík M; Macek M; Lacombe D; Miller K; Moncla A; López Pajares I; Patsalis PC; Petersen MB
    Eur J Hum Genet; 1998; 6(5):432-8. PubMed ID: 9801867
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Methods for analyzing the spatial distribution of chiasmata during meiosis based on recombination data.
    Yu K; Feingold E
    Biometrics; 2002 Jun; 58(2):369-77. PubMed ID: 12071410
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.