Mitotic Recombination of Chromosome Arm 17q as a Cause of Loss of Heterozygosity of NF1 in Neurofibromatosis type 1-associated Glomus Tumors

Neurofibromatosis type 1 (NF1) is a common, autosomal dominant, tumor-predisposition syndrome that arises secondary to mutations in NF1. Glomus tumors are painful benign tumors that originate from the glomus body in the fingers and toes due to biallelic inactivation of NF1. We karyotyped cultures fr...

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Päätekijät: Stewart, Douglas R., Pemov, Alexander, Van Loo, Peter, Beert, Eline, Brems, Hilde, Sciot, Raf, Claes, Kathleen, Pak, Evgenia, Dutra, Amalia, Lee, Chyi-Chia Richard, Legius, Eric
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3295917/
https://ncbi.nlm.nih.gov/pubmed/22250039
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gcc.21928
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