Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

1 Oct 1994

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7927339
DOI: 10.1007/bf00201603

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and livebornsPMID 7927339Read ↗

Etiology of nondisjunction in humansSemantic proximity Read ↗

Nondisjunction in trisomy 21: Origin and mechanismsSemantic proximity Read ↗

The origin of human aneuploidy: where we have been, where we are goingSemantic proximity Read ↗

Trisomy in humans: incidence, origin and etiologySemantic proximity Read ↗

A cytogenetic survey of 14,835 consecutive livebornsSemantic proximity Read ↗

Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic statusSemantic proximity Read ↗

Origin and mechanisms of non-disjunction In human autosomal trisomiesSemantic proximity Read ↗

Aberrant recombination and the origin of Klinefelter syndromeSemantic proximity Read ↗

Chromosome abnormalities and their relationship to morphology and development of human embryosSemantic proximity Read ↗

The origin of trisomy 22: Evidence for acrocentric chromosome‐specific patterns of nondisjunctionSemantic proximity Read ↗

A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.Semantic proximity Read ↗

Chromosome abnormalities in human beingsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.