BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 10798364)

  • 1. 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]  

  • 2. 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]  

  • 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. 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. 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]  

  • 7. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. Down Syndrome Collaborative Group.
    Antonarakis SE
    N Engl J Med; 1991 Mar; 324(13):872-6. PubMed ID: 1825697
    [TBL] [Abstract][Full Text] [Related]  

  • 8. QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe.
    Machatkova M; Brouckova M; Matejckova M; Krebsova A; Sperling K; Vorsanova S; Kutsev S; Zerova T; Arbuzova S; Krejci R; Petersen M; Macek M
    J Histochem Cytochem; 2005 Mar; 53(3):371-3. PubMed ID: 15750023
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK; Hardin EL; Pacheco C; Kuslich CD; Donlon TA
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
    Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW
    Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [The origin of an extra chromosome 21 in families of children with Down syndrome].
    Davidenkova EF; Butomo IV; Kovaleva NV
    Genetika; 1988 Sep; 24(9):1671-8. PubMed ID: 2974006
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of parental origin and cell stage errors of a double nondisjunction in a fetus by QF-PCR.
    Guzel AI; Demirhan O; Pazarbasi A; Ozgunen FT; Kocaturk-Sel S; Tastemir D
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):73-7. PubMed ID: 19309277
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome.
    Viuff MH; Stochholm K; Uldbjerg N; Nielsen BB; ; Gravholt CH
    Hum Reprod; 2015 Oct; 30(10):2419-26. PubMed ID: 26251461
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.