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 *

119 related articles for article (PubMed ID: 6219059)

  • 1. Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study.
    Jongbloet PH; Mulder A; Hamers AJ
    Hum Genet; 1982; 62(2):134-8. PubMed ID: 6219059
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Down syndrome: increased frequency of maternal meiosis I nondisjunction during the transitional stages of the ovulatory seasons.
    Jongbloet PH; Vrieze OJ
    Hum Genet; 1985; 71(3):241-8. PubMed ID: 2933319
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Trisomy 21: origin of non-disjunction.
    del Mazo J; Pérez Castillo A; Abrisqueta JA
    Hum Genet; 1982; 62(4):316-20. PubMed ID: 6219937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. [Age and chromosome nondisjunction].
    Kovaleva NV
    Genetika; 1992 Oct; 28(10):154-61. PubMed ID: 1468638
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Parental alpha 1-antitrypsin (PI) types and meiotic nondisjunction in the aetiology of Down syndrome.
    Jongbloet PH; Frants RR; Hamers AJ
    Clin Genet; 1981 Oct; 20(4):304-9. PubMed ID: 6460570
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A possible cause of non-disjunction of additional chromosome 21 in Down syndrome.
    Verma RS; Babu A; Chemitiganti S; Dosik H
    Mol Gen Genet; 1986 Mar; 202(3):339-41. PubMed ID: 2940437
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunction.
    Soares SR; Templado C; Blanco J; Egozcue J; Vidal F
    Hum Genet; 2001 Feb; 108(2):134-9. PubMed ID: 11281452
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. High efficiency in the attribution of parental origin of non-disjunction in trisomy 21 by both cytogenetic and molecular polymorphisms.
    Bricarelli FD; Pierluigi M; Perroni L; Grasso M; Arslanian A; Sacchi N
    Hum Genet; 1988 Jun; 79(2):124-7. PubMed ID: 2899052
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The parental origin of the extra chromosome 21 in Down's syndrome].
    Hamers AJ; Heijnen GC; Jongbloet PH
    Tijdschr Kindergeneeskd; 1983 Oct; 51(5):157-62. PubMed ID: 6230758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte.
    Halder P; Pal U; Ganguly A; Ghosh P; Ray A; Sarkar S; Ghosh S
    Mol Genet Genomics; 2023 Jan; 298(1):293-313. PubMed ID: 36447056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.