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Article

Genetic alterations in a malignant schwannoma from a patient with neurofibromatosis (NF1).

Pathology, research and practice - 1 May 1993

Lothe R A, Saeter G, Danielsen H E, Stenwig A E, Høyheim B, O'Connell P, Børresen A L

Abstract excerpt

In a patient with neurofibromatosis (von Recklinghausen disease; NF1), normal lymphocytes, five cutaneous neurofibromas, and tumour tissue from a recurrence of a malignant schwannoma were analysed for genetic alterations. Eleven DNA markers located on chromosome 17 and nine randomly chosen markers representing chromosomes 1, 2, 3, 4, 5, 6, and 11, were analysed. High resolution Giemsa banding of lymphocytes...

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Identifiers

PMID: 8351250
DOI: 10.1016/S0344-0338(11)80339-0

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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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