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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1993 1
1994 2
1996 2
2020 0
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Page 1
Trisomy in humans: incidence, origin and etiology.
Hassold T, Hunt PA, Sherman S. Hassold T, et al. Curr Opin Genet Dev. 1993 Jun;3(3):398-403. doi: 10.1016/0959-437x(93)90111-2. Curr Opin Genet Dev. 1993. PMID: 8353412 Review.
Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns.
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Zaragoza MV, et al. Hum Genet. 1994 Oct;94(4):411-7. doi: 10.1007/BF00201603. Hum Genet. 1994. PMID: 7927339
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. Sherman SL, et al. Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529. Hum Mol Genet. 1994. PMID: 7833907
Apolipoprotein E allele distribution in parents of Down's syndrome children.
Avramopoulos D, Mikkelsen M, Vassilopoulos D, Grigoriadou M, Petersen MB. Avramopoulos D, et al. Lancet. 1996 Mar 30;347(9005):862-5. doi: 10.1016/s0140-6736(96)91346-x. Lancet. 1996. PMID: 8622392
Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.
Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, Flanders WD, Khoury MJ, Hassold TJ. Yoon PW, et al. Am J Hum Genet. 1996 Mar;58(3):628-33. Am J Hum Genet. 1996. PMID: 8644722 Free PMC article.
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, et al. Peterson MB, et al. Am J Hum Genet. 1992 Sep;51(3):516-25. Am J Hum Genet. 1992. PMID: 1386710 Free PMC article.