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

Data up to Jan 2025

Published1994
Citations112
References21

Total Citations Per Year

Abstract

References (21)

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

1989 • 887 citations

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

1991 • 278 citations

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

1992 • 194 citations

Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia

1994 • 179 citations

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11–q13): molecular diagnosis and mechanism of uniparental disomy

1993 • 174 citations

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

1991 • 171 citations

Trisomy 21: association between reduced recombination and nondisjunction.

1991 • 169 citations

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

1993 • 147 citations

Nondisjunction of chromosome 15: origin and recombination.

1993 • 109 citations

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

1993 • 102 citations

Cytogenetic and molecular studies of trisomy 13.

1987 • 82 citations

Paternal nondisjunction in trisomy 21: excess of male patients

1993 • 77 citations

The parental origin of the extra X chromosome in 47,XXX females.

1990 • 75 citations

Normal phenotype with paternal uniparental isodisomy for chromosome 21.

1993 • 63 citations

Microsatellite Polymorphism Linkage Map of Human Chromosome 13q

1993 • 60 citations

Molecular studies of non-disjunction in trisomy 16.

1991 • 58 citations

Parental origin of the extra chromosome in trisomy 18.

1989 • 56 citations

Molecular studies of trisomy 18.

1993 • 46 citations

Nondisjunction of chromosome 21

2005 • 43 citations

Trisomy 13 ascertained in a survey of spontaneous abortions.

1987 • 42 citations

Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both

1991 • 32 citations

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Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and… (1994) – Human Genetics | Metascience Observatory Explorer