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

Complementation by two non-homologous recombinant chromosomes 3.

American journal of medical genetics - 15 Jun 1991

Allderdice P W, Ali M, McAlpine P J

Abstract excerpt

The first example known to us of complementation by two non-homologous chromosomes 3 is present in the karyotype of a phenotypically normal brother of an inv(3)(p25q21) carrier. The normal chromosomes 3 are replaced by two complementary recombinant chromosomes 3. The longer recombinant duplicates 3q21-qter and is deficient for 3p25-pter. It is identical to the recombinant inherited by infants born with multiple...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 3
Share to Chromosome Inversion
Share to Genetic Carrier Screening

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Complementation Test

Share to Karyotyping

Share to Phenotype

Share to Recombination, Genetic

Share to Sequence Homology, Nucleic Acid

Source

Identifiers

PMID: 1877616
DOI: 10.1002/ajmg.1320390406

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complementation by two non-homologous recombinant chromosomes 3.PMID 1877616Read ↗

Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryosSemantic proximity Read ↗

Apparent transmission distortion of a pericentric chromosome one inversion in a large multi‐generation pedigreeSemantic proximity Read ↗

Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family.Semantic proximity Read ↗

Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindredSemantic proximity Read ↗

Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loopSemantic proximity Read ↗

A region on chromosome 3 is linked to dizygotic twinning.Semantic proximity Read ↗

Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the LiteratureSemantic proximity Read ↗

Familial complex chromosomal rearrangement resulting in a recombinant chromosomeSemantic proximity Read ↗

Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocationSemantic proximity Read ↗

Different segregation patterns in five carriers due to a pericentric inversion of chromosome 1.Semantic proximity Read ↗

Trisomy 2 due to a 3:1 segregation in an abortion studied by QF‐PCR and CGHSemantic proximity Read ↗

Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities.Semantic proximity Read ↗

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