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 *

149 related articles for article (PubMed ID: 37769135)

  • 21. The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.
    Pal U; Halder P; Ray A; Sarkar S; Datta S; Ghosh P; Ghosh S
    PLoS Genet; 2021 Mar; 17(3):e1009462. PubMed ID: 33750944
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Maternal age effect: the enigma of Down syndrome and other trisomic conditions.
    Gaulden ME
    Mutat Res; 1992 Dec; 296(1-2):69-88. PubMed ID: 1279409
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Origin of trisomy 21 in Down syndrome cases from a Spanish population registry.
    Gómez D; Solsona E; Guitart M; Baena N; Gabau E; Egozcue J; Caballín MR
    Ann Genet; 2000; 43(1):23-8. PubMed ID: 10818217
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Origin of extra chromosome 21 in 343 families: cytogenetic and molecular approaches.
    Dagna Bricarelli F; Pierluigi M; Grasso M; Strigini P; Perroni L
    Am J Med Genet Suppl; 1990; 7():129-32. PubMed ID: 1981472
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Atypical aging in Down syndrome.
    Zigman WB
    Dev Disabil Res Rev; 2013; 18(1):51-67. PubMed ID: 23949829
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.
    Stewart GD; Hassold TJ; Berg A; Watkins P; Tanzi R; Kurnit DM
    Am J Hum Genet; 1988 Feb; 42(2):227-36. PubMed ID: 2893544
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular analysis of nondisjunction in Down syndrome patients with and without atrioventricular septal defects.
    Zittergruen MM; Murray JC; Lauer RM; Burns TL; Sheffield VC
    Circulation; 1995 Nov; 92(10):2803-10. PubMed ID: 7586245
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular Cytogenetic Classification of Down Syndrome and Screening of Somatic Aneuploidy in Mothers.
    Jaiswal SK; Kumar A; Rai AK
    Cytogenet Genome Res; 2021; 161(8-9):397-405. PubMed ID: 34753128
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The origin of aneuploidy: bivalent instability and the maternal age effect in trisomy 21 Down syndrome.
    Hultén MA
    Am J Med Genet Suppl; 1990; 7():160-1. PubMed ID: 2149940
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A fragile X female with Down syndrome.
    Arinami T; Kondo I; Hamaguchi H; Tamura K; Hirano T
    Hum Genet; 1987 Sep; 77(1):92-4. PubMed ID: 2957304
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.
    Peterson MB; Frantzen M; Antonarakis SE; Warren AC; Van Broeckhoven C; Chakravarti A; Cox TK; Lund C; Olsen B; Poulsen H
    Am J Hum Genet; 1992 Sep; 51(3):516-25. PubMed ID: 1386710
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
    Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
    Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
    [TBL] [Abstract][Full Text] [Related]  

  • 36. New insights into human nondisjunction of chromosome 21 in oocytes.
    Oliver TR; Feingold E; Yu K; Cheung V; Tinker S; Yadav-Shah M; Masse N; Sherman SL
    PLoS Genet; 2008 Mar; 4(3):e1000033. PubMed ID: 18369452
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia.
    Lorber BJ; Freeman SB; Hassold T; Ragab AH; Vega RA; Cockwell AE; Jacobs PA; Radford M; Doyle J; Dubé ID
    Genes Chromosomes Cancer; 1992 Apr; 4(3):222-7. PubMed ID: 1382563
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Epidemiology of Down syndrome.
    Sherman SL; Allen EG; Bean LH; Freeman SB
    Ment Retard Dev Disabil Res Rev; 2007; 13(3):221-7. PubMed ID: 17910090
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant].
    Iurov IIu; Vorsanova SG; Monakhov VV; Beresheva AK; Solov'ev IV; Iurov IuB
    Tsitol Genet; 2004; 38(6):54-9. PubMed ID: 15882036
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The pattern of Down syndrome among children in Qatar: a population-based study.
    Wahab AA; Bener A; Sandridge AL; Hoffmann GF
    Birth Defects Res A Clin Mol Teratol; 2006 Aug; 76(8):609-12. PubMed ID: 16955492
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.