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

Translocation 4;13 with adjacent 1 and 3-1 segregations leading to complementary segmental trisomies 13.

Annales de genetique - 1 Jan 1993

Barros-Nuñez P, Higareda O, Cantu J M

Abstract excerpt

A familial 4;13 translocation showed three different segregations and two kinds of imbalances: two brothers had a distal trisomy 13 [46,XY,-4,+der 4, t(4;13)(q35;q14)mat] and their maternal uncle had a proximal trisomy 13 [47, XY,+der13,t(4;13)(q35;q14)mat]. A relative excess of abortions was observed in this family, probably related to a lethal variety of segregation.

Topics

Adult
Chromosome Banding
Chromosome Mapping
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 4
Family
Humans
Infant
Male
Pedigree
Phenotype
Translocation, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Trisomy

Source

Identifiers

PMID: 8117066

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-8117066-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Translocation 4;13 with adjacent 1 and 3-1 segregations leading to complementary segmental trisomies 13.PMID 8117066Read ↗

Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoaSemantic proximity Read ↗

Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event.Semantic proximity Read ↗

Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23).Semantic proximity Read ↗

Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier.Semantic proximity Read ↗

Familial translocation 5;14 resulting in an unbalanced offspring.Semantic proximity Read ↗

The Analysis of Meiotic Segregation Patterns and Aneuploidy in the Spermatozoa of Father and Son With Translocation t(4;5)(p15.1;p12) and the Prediction of the Individual Probability Rate for Unbalanced Progeny at BirthSemantic proximity Read ↗

Molecular studies of translocations and trisomy involving chromosome 13.Semantic proximity Read ↗

Different phenotypes in two cases of an apparently identical familial (Yq;13p) translocation.Semantic proximity Read ↗

Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicismSemantic proximity Read ↗

Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier.Semantic proximity Read ↗

Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literatureSemantic proximity Read ↗

Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of casesSemantic proximity Read ↗

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