Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

Life Sciences, Genetics, Molecular Genetics +11

Parental Origin of the Extra Chromosome in Trisomy 21 as Indicated by Analysis of DNA Polymorphisms

Stylianos E. Antonarakis · New England Journal of Medicine · 1991 · 284 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

Stylianos E. Antonarakis, Dimitrios Avramopoulos, Jean-Louis Blouin et al. · Nature Genetics · 1993 · 218 citations

Life Sciences, Genetics, Molecular Genetics +17

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

Stylianos E. Antonarakis, Michael B. Petersen, Melvin G. McInnis et al. · PubMed · 1992 · 203 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Trisomy 21: association between reduced recombination and nondisjunction.

Stephanie L. Sherman, Norma T. Takaesu, Sallie B. Freeman et al. · PubMed · 1991 · 182 citations

Life Sciences, Genetics, Molecular Genetics +11