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4. 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]
5. 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]
6. [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]
7. Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment. Robinson WP; Bernasconi F; Lau A; McFadden DE Am J Med Genet; 1999 May; 84(1):34-42. PubMed ID: 10213044 [TBL] [Abstract][Full Text] [Related]
9. Analysis of non-disjunction in human trisomic spontaneous abortions. Hassold TJ; Takaesu N Prog Clin Biol Res; 1989; 311():115-34. PubMed ID: 2570425 [No Abstract] [Full Text] [Related]
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. PubMed ID: 17546231 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
14. [Cytogenetic studies of spontaneous abortions in humans]. Zhou CR Zhonghua Fu Chan Ke Za Zhi; 1990 Mar; 25(2):89-91, 124. PubMed ID: 2364797 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Chromosome studies of embryos from induced abortions in pregnant women age 35 and over. Tsuji K; Nakano R Obstet Gynecol; 1978 Nov; 52(5):542-4. PubMed ID: 152877 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. A probability model for the meiosis I non-disjunction fraction in numerical chromosomal anomalies. Franco GC; Lucio PS; Parra FC; Pena SD Stat Med; 2003 Jun; 22(12):2015-24. PubMed ID: 12802819 [TBL] [Abstract][Full Text] [Related]
20. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization. Wolstenholme J Prenat Diagn; 1996 Jun; 16(6):511-24. PubMed ID: 8809892 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]