Discover Community Create You

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

Jumping translocations in spontaneous abortions

1 Jan 2000

Abstract excerpt

Chromosome translocations involving one donor chromosome and multiple recipient chromosomes have been referred to as jumping translocations (JTs). Acquired JTs are commonly observed in cancer patients, mainly involving chromosome 1. Constitutional forms of JTs mostly involve the acrocentric chromosomes and their satellites and have been reported in patients with clinical abnormalities. Recognizable phenotypes...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomal and Genetic Variations
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10773659
DOI: 10.1159/000015478

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Jumping translocations in spontaneous abortionsPMID 10773659Read ↗

Jumping translocation in a phenotypically normal female.Semantic proximity Read ↗

Unstable Robertsonian translocations der(13;15)(q10;q10): Heritable chromosome fission without phenotypic effect in two kindredsSemantic proximity Read ↗

Robertsonian Translocations: Mechanisms of Formation, Aneuploidy, and Uniparental Disomy and Diagnostic ConsiderationsSemantic proximity Read ↗

Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring.Semantic proximity Read ↗

A family with Robertsonian translocation: a potential mechanism of speciation in humansSemantic proximity Read ↗

Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts.Semantic proximity Read ↗

Intrachromosomal triplication for the distal part of chromosome 15q.Semantic proximity Read ↗

Two novel familial balanced translocations t(8;11)(p23;q21) and t(6;16)(q26;p12) implicated in recurrent spontaneous abortion.Semantic proximity Read ↗

Two Novel Cases of Autosomal Translocations in the Horse: Warmblood Family Segregating t(4;30) and a Cloned Arabian with a de novo t(12;25).Semantic proximity Read ↗

Complex chromosome rearrangement with ankyloblepharon filiforme adnatum.Semantic proximity Read ↗

Paracentric inversion inv(18)(q21.1q23) in a woman with recurrent spontaneous abortionsSemantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotypeSemantic proximity Read ↗

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