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Article

Peculiar allelotype associated with susceptibility to neuroblastoma.

Genes, chromosomes & cancer - 1 Sept 1996

Perri P, Pession A, Mazzocco K, Strigini P, Iolascon A, Basso G, Tonini G P

Abstract excerpt

Human neuroblastoma (NB) is characterized genetically by deletions of the short arm of chromosome I and by MYCN amplification. Loss of heterozygosity (LOH) has been found frequently for region 1p36. We have studied restriction fragment length polymorphisms (RFLPs) by using anonymous and hypervariable region (HVR) sequences to demonstrate LOH for 1p loci in 50 Italian neuroblastoma patients. Twelve cases (25%)...

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Source

Identifiers

PMID: 8889508
DOI: 10.1002/(SICI)1098-2264(199609)17:1<60::AID-GCC9>3.0.CO;2-0

Genes

MYCN

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.

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Peculiar allelotype associated with susceptibility to neuroblastoma.PMID 8889508Read ↗

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