The use of molecular genetic analysis in the diagnosis of renal cell carcinoma.

doi:10.1007/BF00184239

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

The use of molecular genetic analysis in the diagnosis of renal cell carcinoma.

World journal of urology - 1 Jan 1994

Long J P, Anglard P, Gnarra J R, Walther M M, Merino M J, Liu S, Lerman M I, Zbar B, Linehan W M

Abstract excerpt

The most common genetic aberration seen in nonpapillary renal cell carcinoma is believed to be the loss or inactivation of allelic material on the short arm of chromosome 3 (3p). Two patients underwent nephrectomy at our institution, each initially receiving a histologic diagnosis of renal cell c...

Topics

Adult
Alleles
Carcinoma, Ductal, Breast
Carcinoma, Renal Cell
Chromosome Aberrations
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 3
DNA Probes
Diagnosis, Differential
Female

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Genetic Carrier Screening

Humans

Kidney Neoplasms

Male

Middle Aged

Molecular Biology

Nephrectomy

Source

Open in PubMed

Identifiers

PMID: 7916238
DOI: 10.1007/BF00184239

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7916238-2026-08-30.1. 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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The use of molecular genetic analysis in the diagnosis of renal cell carcinoma.PMID 7916238Read ↗

Analysis of 3p allelic loss in papillary and nonpapillary renal cell carcinomas. Correlation with tumor karyotypes.Semantic proximity Read ↗

Molecular analysis of the short arm of chromosome 3 in five renal oncocytomas.Semantic proximity Read ↗

Allelic deletions in renal tumors: histopathological correlations.Semantic proximity Read ↗

Comprehensive allelotyping of human renal cell carcinomas using microsatellite DNA probes.Semantic proximity Read ↗

The value of molecular genetic analysis in the diagnosis and prognosis of renal cell tumours.Semantic proximity Read ↗

Chromosome 17p deletions and p53 mutations in renal cell carcinoma.Semantic proximity Read ↗

Application of Chromosome Microarray Analysis for the Differential Diagnosis of Low-grade Renal Cell Carcinoma With Clear Cell and Papillary Features.Semantic proximity Read ↗

Renal cell carcinoma of end-stage renal disease: a histopathologic and molecular genetic study.Semantic proximity Read ↗

Identification of a 700-kb region of common allelic loss in chromosome bands 3p14.3-p21.1 in human renal cell carcinoma.Semantic proximity Read ↗

Genomic alterations and instabilities in renal cell carcinomas and their relationship to tumor pathology.Semantic proximity Read ↗

Deletion mapping on the short arm of chromosome 3 in squamous cell carcinoma and adenocarcinoma of the lung.Semantic proximity Read ↗

Combined classical cytogenetics and microarray‐based genomic copy number analysis reveal frequent 3;5 rearrangements in clear cell renal cell carcinomaSemantic proximity Read ↗

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