Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2. Jo, R., Sabine, S., Frank, H., Jean-François, B., Lieve, B., Teofila, C., Kathleen, C., Eric, L., Sylvie, R., Dirk, S., Daphné, t. d. R., Tom, v. M., Urielle, U., & Kris, P. Technical Report Belgian Health Care Knowledge Centre (KCE), Brussels, 2015.
Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2 [pdf]Paper  bibtex   

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