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

Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.

Annals of human genetics - 1 Sept 1996

Tomlinson I P, Olschwang S, Abelovitch D, Nakamura Y, Bodmer W F, Thomas G, Markie D

Abstract excerpt

Peutz-Jeghers' syndrome (PJS) is a disease with autosomal dominant inheritance, which is characterised by gastrointestinal hamartomata and characteristic melanin pigmentation. Three candidate sites for a PJS locus have recently been proposed, chromosomes 1p31-p32, 6q25 and 6p11-cen. At the first of these sites, a multipoint LOD score of 4.00 had been found, strongly suggesting genetic linkage to PJS. The last two...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 1
Share to France
Share to Genotype

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

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Lod Score

Share to Pedigree

Source

Identifiers

PMID: 8912790
DOI: 10.1111/j.1469-1809.1996.tb00435.x

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

Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease.PMID 8912790Read ↗

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.Semantic proximity Read ↗

Peutz-Jeghers syndrome.Semantic proximity Read ↗

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.Semantic proximity Read ↗

No evidence of linkage between 7q33-36 locus (OTSC2) and otosclerosis in seven British Caucasian pedigrees.Semantic proximity Read ↗

Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22.Semantic proximity Read ↗

Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p.Semantic proximity Read ↗

Linkage of inflammatory bowel disease to human chromosome 6p.Semantic proximity Read ↗

Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2.Semantic proximity Read ↗

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qSemantic proximity Read ↗

Linkage analysis of familial melanoma and chromosome 6 in 14 Australian kindreds.Semantic proximity Read ↗

Linkage study of chromosome 6p in sib-pairs with schizophrenia.Semantic proximity Read ↗

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease.Semantic proximity Read ↗

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