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

T(In1;5)44H, a complex mouse chromosomal rearrangement with a phenotypic effect.

Cytogenetics and cell genetics - 1 Jan 1993

Evans E P, Beechey C V, Burtenshaw M D, Searle A G

Abstract excerpt

A complex murine chromosomal rearrangement, T(In1;5)44H, was recovered after 5 Gy + 5 Gy (given 24 h apart) spermatogonial X-irradiation. T44H is a paracentric inversion of most of Chromosome (Chr) 1 (1A1-1H6), followed by splitting of the inverted segment through a reciprocal translocation with...

Topics

Animals
Chromosome Aberrations
Chromosome Disorders
Chromosome Inversion
Female
Genetic Linkage
Heterozygote
Infertility, Female
Karyotyping
Litter Size
Male
Meiosis
Mice

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Spermatozoa

Translocation, Genetic

Source

Identifiers

PMID: 8449042
DOI: 10.1159/000133506

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8449042-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 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

T(In1;5)44H, a complex mouse chromosomal rearrangement with a phenotypic effect.PMID 8449042Read ↗

Genetic and molecular evidence of an X-chromosome deletion spanning the tabby (Ta) and testicular feminization (Tfm) loci in the mouse.Semantic proximity Read ↗

QTL on mouse chromosomes 1 and 4 causing sperm-head morphological abnormality and male subfertility.Semantic proximity Read ↗

Mouse chromosome 5.Semantic proximity Read ↗

Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene.Semantic proximity Read ↗

Gnome and other effects of a small translocation in the mouse.Semantic proximity Read ↗

Etoposide induces heritable chromosomal aberrations and aneuploidy during male meiosis in the mouseSemantic proximity Read ↗

Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.Semantic proximity Read ↗

Mapping of the azh locus to mouse chromosome 4.Semantic proximity Read ↗

Determination of a molecular map position for Hyp using a new interspecific backcross produced by in vitro fertilization.Semantic proximity Read ↗

Faint lined (Fnl): a novel X-linked coat mutant in the mouse.Semantic proximity Read ↗

Genetic analysis of X-linked hybrid sterility in the house mouse.Semantic proximity Read ↗

Transfer of a Mouse Artificial Chromosome into Spermatogonial Stem Cells Generates Transchromosomic Mice.Semantic proximity Read ↗

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