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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 hypervari...

Topics

Alleles
Chromosome Deletion
Chromosomes, Human, Pair 1
Gene Amplification
Gene Frequency
Heterozygote
Humans
Neuroblastoma

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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 30 Aug 2026. Prepared record publication-8889508-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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

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