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. Paper bibtex @techreport{jo_oncogenetic_2015-1,
address = {Brussels},
type = {Good {Clinical} {Practice} ({GCP})},
title = {Oncogenetic testing, diagnosis and follow-up in {Birt}-{Hogg}-{Dubé} syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2},
url = {http://kce.fgov.be/sites/default/files/page_documents/KCE_243_oncogenetic_testing_Neurofibromatosis_Report.pdf},
institution = {Belgian Health Care Knowledge Centre (KCE)},
author = {Jo, Robays and Sabine, Stordeur and Frank, Hulstaert and Jean-François, Baurain and Lieve, Brochez and Teofila, Caplanusi and Kathleen, Claes and Eric, Legius and Sylvie, Rottey and Dirk, Schrijvers and Daphné, t'Kint de Roodenbeke and Tom, van Maerken and Urielle, Ullman and Kris, Poppe},
year = {2015},
keywords = {Neurofibromatoses}
}
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