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 *

219 related articles for article (PubMed ID: 15849793)

  • 1. A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.
    Chen CP; Chern SR; Tsai FJ; Lin CY; Lin YH; Wang W
    Prenat Diagn; 2005 Apr; 25(4):327-30. PubMed ID: 15849793
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Non-disjunction of chromosome 13.
    Bugge M; Collins A; Hertz JM; Eiberg H; Lundsteen C; Brandt CA; Bak M; Hansen C; Delozier CD; Lespinasse J; Tranebjaerg L; Hahnemann JM; Rasmussen K; Bruun-Petersen G; Duprez L; Tommerup N; Petersen MB
    Hum Mol Genet; 2007 Aug; 16(16):2004-10. PubMed ID: 17584770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II.
    Lamb NE; Freeman SB; Savage-Austin A; Pettay D; Taft L; Hersey J; Gu Y; Shen J; Saker D; May KM; Avramopoulos D; Petersen MB; Hallberg A; Mikkelsen M; Hassold TJ; Sherman SL
    Nat Genet; 1996 Dec; 14(4):400-5. PubMed ID: 8944019
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
    Bornstein E; Barnhard Y; Donnenfeld A; Ferber A; Divon MY
    Obstet Gynecol; 2006 Apr; 107(4):877-9. PubMed ID: 16582126
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. Advanced parental age in maternal uniparental disomy (UPD): implications for the mechanism of formation.
    Kotzot D
    Eur J Hum Genet; 2004 May; 12(5):343-6. PubMed ID: 14747835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sex ratios in fetuses and liveborn infants with autosomal aneuploidy.
    Huether CA; Martin RL; Stoppelman SM; D'Souza S; Bishop JK; Torfs CP; Lorey F; May KM; Hanna JS; Baird PA; Kelly JC
    Am J Med Genet; 1996 Jun; 63(3):492-500. PubMed ID: 8737659
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.
    Diego-Alvarez D; Ramos-Corrales C; Garcia-Hoyos M; Bustamante-Aragones A; Cantalapiedra D; Diaz-Recasens J; Vallespin-Garcia E; Ayuso C; Lorda-Sanchez I
    Hum Reprod; 2006 Apr; 21(4):958-66. PubMed ID: 16361293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
    Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
    Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.
    Juberg RC; Mowrey PN
    Am J Med Genet; 1983 Sep; 16(1):111-6. PubMed ID: 6227238
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases.
    Yaegashi N; Senoo M; Uehara S; Suzuki H; Maeda T; Fujimori K; Hirahara F; Yajima A
    J Hum Genet; 1998; 43(2):85-90. PubMed ID: 9621511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.
    Yoon PW; Freeman SB; Sherman SL; Taft LF; Gu Y; Pettay D; Flanders WD; Khoury MJ; Hassold TJ
    Am J Hum Genet; 1996 Mar; 58(3):628-33. PubMed ID: 8644722
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
    Chen CP; Chern SR; Chen CY; Wu PC; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):479-84. PubMed ID: 22212321
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion.
    Li QY; Tsukishiro S; Nakagawa C; Tanemura M; Sugiura-Ogasawara M; Suzumori K; Sonta S
    Congenit Anom (Kyoto); 2005 Mar; 45(1):21-5. PubMed ID: 15737127
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.