Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.

doi:10.1002/gcc.2870050416

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

Back to search

Article

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.

Genes, chromosomes & cancer - 1 Nov 1992

Tanaka N, Nishisho I, Yamamoto M, Miya A, Shin E, Karakawa K, Fujita S, Kobayashi T, Rouleau G A, Mori T

Abstract excerpt

To identify the putative common deleted region on the long arm of chromosome 22 in pheochromocytoma, restriction fragment length polymorphism analysis was performed in 17 pheochromocytomas. All cases were heterozygous for at least one of the eight marker loci on 22q. Loss of heterozygosity (LOH)...

Topics

Adrenal Gland Neoplasms
Alleles
Carcinoma
Chromosome Aberrations
Chromosomes, Human, Pair 22
DNA Probes
Gene Deletion
Genes, Neurofibromatosis 2
Genes, Tumor Suppressor
Genetic Markers
Humans
Meningeal Neoplasms
Meningioma
Multiple Endocrine Neoplasia
Neurofibromatosis 2

Source

Open in PubMed

Identifiers

PMID: 1283329
DOI: 10.1002/gcc.2870050416

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-1283329-2026-08-30.1. 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.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Pheochromocytoma

Polymorphism, Restriction Fragment Length

Thyroid Neoplasms