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 *

455 related articles for article (PubMed ID: 9557829)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.
    Thomas NS; Ennis S; Sharp AJ; Durkie M; Hassold TJ; Collins AR; Jacobs PA
    Hum Mol Genet; 2001 Feb; 10(3):243-50. PubMed ID: 11159943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Parental origin of autosomal trisomies.
    Hassold T; Chiu D; Yamane JA
    Ann Hum Genet; 1984 May; 48(2):129-44. PubMed ID: 6234852
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Non-disjunction of chromosome 18.
    Bugge M; Collins A; Petersen MB; Fisher J; Brandt C; Hertz JM; Tranebjaerg L; de Lozier-Blanchet C; Nicolaides P; Brøndum-Nielsen K; Morton N; Mikkelsen M
    Hum Mol Genet; 1998 Apr; 7(4):661-9. PubMed ID: 9499419
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.
    Vorsanova SG; Iourov IY; Beresheva AK; Demidova IA; Monakhov VV; Kravets VS; Bartseva OB; Goyko EA; Soloviev IV; Yurov YB
    Tsitol Genet; 2005; 39(6):30-6. PubMed ID: 16396318
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities.
    Baidas S; Chen TJ; Kolev V; Wong LJ; Imholte J; Qin N; Meck J
    Am J Med Genet A; 2004 Feb; 124A(4):383-7. PubMed ID: 14735586
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.
    Sherman SL; Petersen MB; Freeman SB; Hersey J; Pettay D; Taft L; Frantzen M; Mikkelsen M; Hassold TJ
    Hum Mol Genet; 1994 Sep; 3(9):1529-35. PubMed ID: 7833907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Molecular studies of non-disjunction in trisomy 16.
    Hassold TJ; Pettay D; Freeman SB; Grantham M; Takaesu N
    J Med Genet; 1991 Mar; 28(3):159-62. PubMed ID: 2051452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombination.
    Robinson WP; Kuchinka BD; Bernasconi F; Petersen MB; Schulze A; Brondum-Nielsen K; Christian SL; Ledbetter DH; Schinzel AA; Horsthemke B; Schuffenhauer S; Michaelis RC; Langlois S; Hassold TJ
    Hum Mol Genet; 1998 Jun; 7(6):1011-9. PubMed ID: 9580665
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of the origin of the extra chromosome in trisomy 8 in 4 cases of spontaneous abortions.
    Nicolaidis P; von Beust G; Bugge M; Karadima G; Vassilopoulos D; Brøndum-Nielsen K; Petersen MB
    Fetal Diagn Ther; 1998; 13(1):42-5. PubMed ID: 9605616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data.
    Ghosh S; Bhaumik P; Ghosh P; Dey SK
    Genet Res (Camb); 2010 Jun; 92(3):189-97. PubMed ID: 20667163
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.