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Genes, Neurofibromatosis 1

"Genes, Neurofibromatosis 1" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

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Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.

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This graph shows the total number of publications written about "Genes, Neurofibromatosis 1" by people in UAMS Profiles by year, and whether "Genes, Neurofibromatosis 1" was a major or minor topic of these publications.
Bar chart showing 3 publications over 3 distinct years, with a maximum of 1 publications in 2000 and 2005 and 2011
To see the data from this visualization as text, click here.