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

Genetic studies of a family with hereditary hyperparathyroidism–jaw tumour syndrome

1 Feb 1999

Abstract excerpt

BACKGROUND AND OBJECTIVES: Familial hyperparathyroidism may occur as familial isolated hyperparathyroidism (FIHP) or as part of an inherited syndrome, in particular multiple endocrine neoplasia types 1 and 2A (MEN1, MEN2A) and hyperparathyroidism-jaw tumour (HPT-JT) syndrome. The localization of the genes responsible for these syndromes has enabled genetic screening of families with primary hyperparathyroidism...

Read the complete abstract on PubMed

Topics

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

Share to Bone health and treatments
Share to Neuroendocrine Tumor Research Advances
Share to Parathyroid Disorders and Treatments

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

Source

Identifiers

PMID: 10396361
DOI: 10.1046/j.1365-2265.1999.00633.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

Genetic studies of a family with hereditary hyperparathyroidism–jaw tumour syndromePMID 10396361Read ↗

Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.Semantic proximity Read ↗

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.Semantic proximity Read ↗

Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.Semantic proximity Read ↗

A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.Semantic proximity Read ↗

A Genotypic and Histopathological Study of a Large Dutch Kindred with Hyperparathyroidism-Jaw Tumor SyndromeSemantic proximity Read ↗

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene.Semantic proximity Read ↗

Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome.Semantic proximity Read ↗

Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management.Semantic proximity Read ↗

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.Semantic proximity Read ↗

The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindredSemantic proximity Read ↗

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.Semantic proximity Read ↗

Hereditary hyperparathyroidism--a consensus report of the European Society of Endocrine Surgeons (ESES).Semantic proximity Read ↗

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