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Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.

Hollis ND, Allen EG, Oliver TR, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL, Bean LJ.

Am J Med Genet A. 2013 Mar;161A(3):438-44. doi: 10.1002/ajmg.a.35796. Epub 2013 Feb 7.


Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.

Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL.

Hum Genet. 2009 Feb;125(1):41-52. doi: 10.1007/s00439-008-0603-8. Epub 2008 Dec 3.


The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.

Hunter JE, Allen EG, Shin M, Bean LJ, Correa A, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL.

Genet Med. 2013 Sep;15(9):698-705. doi: 10.1038/gim.2013.34. Epub 2013 Apr 4.


Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.

Bean LJ, Allen EG, Tinker SW, Hollis ND, Locke AE, Druschel C, Hobbs CA, O'Leary L, Romitti PA, Royle MH, Torfs CP, Dooley KJ, Freeman SB, Sherman SL.

Birth Defects Res A Clin Mol Teratol. 2011 Oct;91(10):885-93. doi: 10.1002/bdra.22848. Epub 2011 Aug 24.


Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth.

Ghosh S, Feingold E, Chakraborty S, Dey SK.

Hum Genet. 2010 Apr;127(4):403-9. doi: 10.1007/s00439-009-0785-8.


Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome.

James SJ, Pogribna M, Pogribny IP, Melnyk S, Hine RJ, Gibson JB, Yi P, Tafoya DL, Swenson DH, Wilson VL, Gaylor DW.

Am J Clin Nutr. 1999 Oct;70(4):495-501.


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 14;4(3):e1000033. doi: 10.1371/journal.pgen.1000033.


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, et al.

Am J Hum Genet. 1992 Mar;50(3):544-50.


Pre-conceptional vitamin/folic acid supplementation 2007: the use of folic acid in combination with a multivitamin supplement for the prevention of neural tube defects and other congenital anomalies.

Wilson RD, Johnson JA, Wyatt P, Allen V, Gagnon A, Langlois S, Blight C, Audibert F, Désilets V, Brock JA, Koren G, Goh YI, Nguyen P, Kapur B; Genetics Committee of the Society of Obstetricians and Gynaecologists of Canada and The Motherrisk Program.

J Obstet Gynaecol Can. 2007 Dec;29(12):1003-26. English, French. Erratum in: J Obstet Gynaecol Can. 2008 Mar;30(3):193. Goh, Ingrid [corrected to Goh, Y Ingrid].


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 15;92(10):2803-10.


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. Epub 2007 May 31.


Nondisjunction in trisomy 21: origin and mechanisms.

Petersen MB, Mikkelsen M.

Cytogenet Cell Genet. 2000;91(1-4):199-203. Review.


Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status.

Christianson RE, Sherman SL, Torfs CP.

Genet Med. 2004 Nov-Dec;6(6):487-94.


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. doi: 10.1017/S0016672310000224.


Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida.

Shaw GM, Rozen R, Finnell RH, Wasserman CR, Lammer EJ.

Am J Epidemiol. 1998 Jul 1;148(1):30-7.


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.


Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects.

Pei L, Liu J, Zhang Y, Zhu H, Ren A.

Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):874-8. doi: 10.1002/ajmg.b.30911.

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