BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 8116616)

  • 1. 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]  

  • 2. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.
    Antonarakis SE; Petersen MB; McInnis MG; Adelsberger PA; Schinzel AA; Binkert F; Pangalos C; Raoul O; Slaugenhaupt SA; Hafez M
    Am J Hum Genet; 1992 Mar; 50(3):544-50. PubMed ID: 1347192
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age.
    Antonarakis SE; Avramopoulos D; Blouin JL; Talbot CC; Schinzel AA
    Nat Genet; 1993 Feb; 3(2):146-50. PubMed ID: 8499948
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Parental age and the origin of extra chromosome 21 in Down syndrome.
    Jyothy A; Kumar KS; Mallikarjuna GN; Babu Rao V; Uma Devi B; Sujatha M; Reddy PP
    J Hum Genet; 2001; 46(6):347-50. PubMed ID: 11393539
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.
    Ikonen RS; Lindlöf M; Janas MO; Simola KO; Millington-Ward A; de la Chapelle A
    Hum Genet; 1989 Oct; 83(3):235-8. PubMed ID: 2571561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA polymorphism analysis in families with recurrence of free trisomy 21.
    Pangalos CG; Talbot CC; Lewis JG; Adelsberger PA; Petersen MB; Serre JL; Rethoré MO; de Blois MC; Parent P; Schinzel AA
    Am J Hum Genet; 1992 Nov; 51(5):1015-27. PubMed ID: 1415248
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches.
    Dagna Bricarelli F; Pierluigi M; Grasso M; Strigini P; Perroni L
    Am J Med Genet Suppl; 1990; 7():129-32. PubMed ID: 1981472
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.
    Ballesta F; Queralt R; Gómez D; Solsona E; Guitart M; Ezquerra M; Moreno J; Oliva R
    Ann Genet; 1999; 42(1):11-5. PubMed ID: 10214502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nondisjunction of chromosome 21.
    Takaesu N; Jacobs PA; Cockwell A; Blackston RD; Freeman S; Nuccio J; Kurnit DM; Uchida I; Freeman V; Hassold T
    Am J Med Genet Suppl; 1990; 7():175-81. PubMed ID: 1981476
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.
    Berend SA; Page SL; Atkinson W; McCaskill C; Lamb NE; Sherman SL; Shaffer LG
    Am J Hum Genet; 2003 Feb; 72(2):488-95. PubMed ID: 12506337
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.
    Petersen MB; Adelsberger PA; Schinzel AA; Binkert F; Hinkel GK; Antonarakis SE
    Am J Hum Genet; 1991 Sep; 49(3):529-36. PubMed ID: 1831959
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Paternal nondisjunction in trisomy 21: excess of male patients.
    Petersen MB; Antonarakis SE; Hassold TJ; Freeman SB; Sherman SL; Avramopoulos D; Mikkelsen M
    Hum Mol Genet; 1993 Oct; 2(10):1691-5. PubMed ID: 8268923
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Paternal meiotic origin of der(21;21)(q10;q10) mosaicism [46,XX/46, XX,der(21;21)(q10;q10),+21] in a girl with mild Down syndrome.
    Kotzot D; Schinzel A
    Eur J Hum Genet; 2000 Sep; 8(9):709-12. PubMed ID: 10980577
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The origin of mosaic Down syndrome: four cases with chromosome markers.
    Niikawa N; Kajii T
    Am J Hum Genet; 1984 Jan; 36(1):123-30. PubMed ID: 6230008
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Confined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer.
    Valind A; Pal N; Asmundsson J; Gisselsson D; Holmquist Mengelbier L
    Genes Chromosomes Cancer; 2014 Jul; 53(7):634-8. PubMed ID: 24729308
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Origin of trisomy 21 in Down syndrome cases from a Spanish population registry.
    Gómez D; Solsona E; Guitart M; Baena N; Gabau E; Egozcue J; Caballín MR
    Ann Genet; 2000; 43(1):23-8. PubMed ID: 10818217
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.