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Article

Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1

13 May 2020

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32405727
DOI: 10.1007/s10689-020-00184-3

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Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1PMID 32405727Read ↗

Integrative Genomic and Functional Analysis Reveals NF1 Loss as a Modifier of DNA Damage and Replication Stress Responses in Ovarian Cancer.Semantic proximity Read ↗

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Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 mutations.Semantic proximity Read ↗

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Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma.Semantic proximity Read ↗

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of <i>NF1</i> in neurofibromatosis type 1‐associated glomus tumorsSemantic proximity Read ↗

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NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific ProbesSemantic proximity Read ↗

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