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 *

116 related articles for article (PubMed ID: 8659537)

  • 41. Molecular basis of maternal age-related increase in oocyte aneuploidy.
    Kurahashi H; Tsutsumi M; Nishiyama S; Kogo H; Inagaki H; Ohye T
    Congenit Anom (Kyoto); 2012 Mar; 52(1):8-15. PubMed ID: 22348779
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects.
    Zittergruen MM; Murray JC; Lauer RM; Burns TL; Sheffield VC
    Circulation; 1995 Nov; 92(10):2803-10. PubMed ID: 7586245
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Parental origin of the extra chromosome in Down's syndrome.
    Magenis RE; Overton KM; Chamberlin J; Brady T; Lovrien E
    Hum Genet; 1977 Jun; 37(1):7-16. PubMed ID: 142063
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.
    Pangalos C; Avramopoulos D; Blouin JL; Raoul O; deBlois MC; Prieur M; Schinzel AA; Gika M; Abazis D; Antonarakis SE
    Am J Hum Genet; 1994 Mar; 54(3):473-81. PubMed ID: 8116616
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Meiosis I non-disjunction as the main cause of trisomy 21.
    Robinson JA
    Hum Genet; 1977 Nov; 39(1):27-30. PubMed ID: 144698
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Trisomy 21: fifty years between medicine and science].
    Turleau C; Vekemans M
    Med Sci (Paris); 2010 Mar; 26(3):267-72. PubMed ID: 20346276
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Attrition of trisomies as a maternal screening device. An explanation of the association of trisomy 21 with maternal age.
    Stein Z; Stein W; Susser M
    Lancet; 1986 Apr; 1(8487):944-7. PubMed ID: 2871243
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A chiasma-hormonal hypothesis relating Down's syndrome and maternal age.
    Crowley PH; Gulati DK; Hayden TL; Lopez P; Dyer R
    Nature; 1979 Aug; 280(5721):417-8. PubMed ID: 156882
    [No Abstract]   [Full Text] [Related]  

  • 49. The origin of trisomy in humans.
    Hassold T; Sherman S; Hunt PA
    Prog Clin Biol Res; 1995; 393():1-12. PubMed ID: 8545442
    [No Abstract]   [Full Text] [Related]  

  • 50. Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.
    Ramírez NJ; Belalcázar HM; Yunis JJ; Quintero LN; Arboleda GH; Arboleda H
    Biomedica; 2007 Mar; 27(1):141-8. PubMed ID: 17546231
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Parental age-related aneuploidy in human germ cells and offspring: a story of past and present.
    Eichenlaub-Ritter U
    Environ Mol Mutagen; 1996; 28(3):211-36. PubMed ID: 8908181
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
    Bruyère H; Rupps R; Kuchinka BD; Friedman JM; Robinson WP
    Am J Med Genet; 2000 Sep; 94(1):35-41. PubMed ID: 10982480
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [On the origin of meiotic errors with special reference to trisomy 21 (author's transl)].
    Wagenbichler P
    Wien Klin Wochenschr Suppl; 1976; 63():1-23. PubMed ID: 136814
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Down's syndrome in twins (according to the study of 15 pairs)].
    Badalian LO; Lipovetskaia NG; Oradovskaia IV
    Pediatriia; 1974 Mar; 3():46-55. PubMed ID: 4275143
    [No Abstract]   [Full Text] [Related]  

  • 55. Alzheimer's disease and down syndrome: from meiosis to dementia.
    Petronis A
    Exp Neurol; 1999 Aug; 158(2):403-13. PubMed ID: 10415146
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome.
    Petersen MB; Karadima G; Samaritaki M; Avramopoulos D; Vassilopoulos D; Mikkelsen M
    Am J Med Genet; 2000 Aug; 93(5):366-72. PubMed ID: 10951459
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Down anomaly: new research aspects of an old and well known syndrome.
    Mikkelsen M
    Prog Clin Biol Res; 1985; 177():293-307. PubMed ID: 3160045
    [No Abstract]   [Full Text] [Related]  

  • 58. The single nucleotide polymorphism (80G-->A) of reduced folate carrier gene in trisomy 21.
    Chango A; Willequet F; Fillon-Emery N; Nicolas JP; Bléhaut H
    Am J Clin Nutr; 2004 Dec; 80(6):1667-9. PubMed ID: 15585786
    [No Abstract]   [Full Text] [Related]  

  • 59. Women with a reduced ovarian complement may have an increased risk for a child with Down syndrome.
    Freeman SB; Yang Q; Allran K; Taft LF; Sherman SL
    Am J Hum Genet; 2000 May; 66(5):1680-3. PubMed ID: 10733467
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 6.