BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

258 related articles for article (PubMed ID: 8566957)

  • 1. 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]  

  • 2. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.
    Zaragoza MV; Jacobs PA; James RS; Rogan P; Sherman S; Hassold T
    Hum Genet; 1994 Oct; 94(4):411-7. PubMed ID: 7927339
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Parental origin of the extra chromosome 18 in Edwards syndrome.
    Ramesh KH; Verma RS
    Ann Genet; 1996; 39(2):110-2. PubMed ID: 8766143
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reduced recombination and paternal age effect in Klinefelter syndrome.
    Lorda-Sanchez I; Binkert F; Maechler M; Robinson WP; Schinzel AA
    Hum Genet; 1992 Jul; 89(5):524-30. PubMed ID: 1353053
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Origin of extra chromosome in Patau syndrome.
    Ishikiriyama S; Niikawa N
    Hum Genet; 1984; 68(3):266-8. PubMed ID: 6500580
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Parental origin of the supernumerary chromosome in trisomy 18.
    Ya-gang X; Robinson WP; Spiegel R; Binkert F; Ruefenacht U; Schinzel AA
    Clin Genet; 1993 Aug; 44(2):57-61. PubMed ID: 8275560
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction.
    Fisher JM; Harvey JF; Morton NE; Jacobs PA
    Am J Hum Genet; 1995 Mar; 56(3):669-75. PubMed ID: 7887421
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.
    Hall HE; Surti U; Hoffner L; Shirley S; Feingold E; Hassold T
    Am J Med Genet A; 2007 Oct; 143A(19):2249-55. PubMed ID: 17705154
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isochromosome 18p results from maternal meiosis II nondisjunction.
    Kotzot D; Bundscherer G; Bernasconi F; Brecevic L; Lurie IW; Basaran S; Baccicchetti C; Höller A; Castellan C; Braun-Quentin C; Pfeiffer RA; Schinzel A
    Eur J Hum Genet; 1996; 4(3):168-74. PubMed ID: 8840117
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21.
    Muller F; Rebiffé M; Taillandier A; Oury JF; Mornet E
    Hum Genet; 2000 Mar; 106(3):340-4. PubMed ID: 10798364
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomies.
    Brahe C; Tassone F; Moscetti A; Millington-Ward A; Bova R; Serra A
    Am J Med Genet Suppl; 1990; 7():125-8. PubMed ID: 2149938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
    Eggermann T; Schubert R; Engels H; Apacik C; Stengel-Rutkowski S; Haefliger C; Emiliani V; Ricagni C; Schwanitz G
    Ann Genet; 1999; 42(2):75-80. PubMed ID: 10434120
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Risk of Down syndrome birth: Consanguineous marriage is associated with maternal meiosis-II nondisjunction at younger age and without any detectable recombination error.
    Ray A; Oliver TR; Halder P; Pal U; Sarkar S; Dutta S; Ghosh S
    Am J Med Genet A; 2018 Nov; 176(11):2342-2349. PubMed ID: 30240118
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.