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[Familial atypical multiple mole melanoma syndrome--FAMMM].
Foretová L, Macháková E, Sachlová M, Petráková K, Palácová M. Foretová L, et al. Among authors: machakova e. Klin Onkol. 2009;22 Suppl:S32-3. Klin Onkol. 2009. PMID: 19764392 Review. Czech. No abstract available.
ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes.
Spurdle AB, Healey S, Devereau A, Hogervorst FB, Monteiro AN, Nathanson KL, Radice P, Stoppa-Lyonnet D, Tavtigian S, Wappenschmidt B, Couch FJ, Goldgar DE; ENIGMA. Spurdle AB, et al. Hum Mutat. 2012 Jan;33(1):2-7. doi: 10.1002/humu.21628. Epub 2011 Nov 3. Hum Mutat. 2012. PMID: 21990146 Free PMC article.