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Article

Trisomy 7 and 17 mark papillary renal cell tumours irrespectively of variation of the phenotype.

Journal of clinical pathology - 1 Oct 2009

Balint I, Szponar A, Jauch A, Kovacs G

Abstract excerpt

BACKGROUND: Papillary renal cell tumours (RCTs) have been described as a genetic entity. Recently, papillary RCTs have been divided into small (type 1) and large (type 2) cell tumours. Subsequent DNA analyses have resulted in controversial data regarding putative genetic changes marking type 1 and type 2 tumours. AIM: The aim of this study was to improve the original description that papillary RCT is a genetic...

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Share to Carcinoma, Papillary
Share to Chromosomes, Human, Pair 17
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19541684
DOI: 10.1136/jcp.2009.066423

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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.

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