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

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

Human genetics - 1 Mar 1999

Baysal B E, van Schothorst E M, Farr J E, Grashof P, Myssiorek D, Rubinstein W S, Taschner P, Cornelisse C J, Devlin B, Devilee P, Richard C W

Abstract excerpt

Hereditary paragangliomas (PGL, glomus tumors, MIM no.168000) are mostly benign, slow-growing tumors of the head and neck region. The gene (or genes) affecting risk to PGL are subject to genomic imprinting: children of affected fathers exhibit an autosomal dominant pattern of disease inheritance, whereas children of affected mothers rarely if ever develop the disease through maternal transmission. We previously...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Banding
Share to Chromosome Mapping

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

Share to Chromosomes, Human, Pair 11

Share to Family Health

Share to Genetic Markers

Share to Haplotypes

Share to Head and Neck Neoplasms

Share to Paraganglioma

Source

Identifiers

PMID: 10323245
DOI: 10.1007/s004390050939

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

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.PMID 10323245Read ↗

A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.Semantic proximity Read ↗

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.Semantic proximity Read ↗

Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.Semantic proximity Read ↗

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qterSemantic proximity Read ↗

Genetics of familial paragangliomas: past, present, and future.Semantic proximity Read ↗

A Novel Targeted Sequence for Chromosome 11p15.5 Maternal Loss in SDHD-Related Paragangliomas.Semantic proximity Read ↗

Genetic Analysis in the Diagnosis of Familial ParagangliomasSemantic proximity Read ↗

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.Semantic proximity Read ↗

Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paragangliomaSemantic proximity Read ↗

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneitySemantic proximity Read ↗

Are head and neck versus abdominal paragangliomas driven by different single nucleotide events?Semantic proximity Read ↗

Abdominal paraganglioma in a young woman with 1p36 deletion syndrome.Semantic proximity Read ↗

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