A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma

BACKGROUND: Association of melanoma, neural system tumors and germ line mutations at the 9p21 region in the CDKN2A, CDKN2B and CDKN2BAS genes has been reported in a small number of families worldwide and described as a discrete syndrome in melanoma families registered as a rare disease, the melanoma...

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Bibliografische gegevens
Hoofdauteurs: Frigerio, Simona, Disciglio, Vittoria, Manoukian, Siranoush, Peissel, Bernard, Della Torre, Gabriella, Maurichi, Andrea, Collini, Paola, Pasini, Barbara, Gotti, Giacomo, Ferrari, Andrea, Rivoltini, Licia, Massimino, Maura, Rodolfo, Monica
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2014
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Case Report
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4036080/
https://ncbi.nlm.nih.gov/pubmed/24884915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-15-59
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