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Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2

(2015) KCE Report. 243.
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MLA
Robays, Jo, et al. “Oncogenetic Testing, Diagnosis and Follow-up in Birt-Hogg-Dubé Syndrome, Familial Atypical Multiple Mole Melanoma Syndrome and Neurofibromatosis 1 and 2.” KCE Report, vol. 243, Federaal Kenniscentrum voor de Gezondheidszorg (KCE), 2015.
APA
Robays, J., Stordeur, S., Hulstaert, F., Baurain, J.-F., Brochez, L., Caplanusi, T., … Poppe, B. (2015). Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2. KCE Report. Brussels, Belgium: Federaal Kenniscentrum voor de Gezondheidszorg (KCE).
Chicago author-date
Robays, Jo, Sabine Stordeur, Frank Hulstaert, Jean-François Baurain, Lieve Brochez, Teofila Caplanusi, Kathleen Claes, et al. 2015. “Oncogenetic Testing, Diagnosis and Follow-up in Birt-Hogg-Dubé Syndrome, Familial Atypical Multiple Mole Melanoma Syndrome and Neurofibromatosis 1 and 2.” KCE Report. Brussels, Belgium: Federaal Kenniscentrum voor de Gezondheidszorg (KCE).
Chicago author-date (all authors)
Robays, Jo, Sabine Stordeur, Frank Hulstaert, Jean-François Baurain, Lieve Brochez, Teofila Caplanusi, Kathleen Claes, Eric Legius, Sylvie Rottey, Dirk Schrijvers, Daphné ’t Kint de Roodenbeke, Urielle Ullman, Tom Van Maerken, and Bruce Poppe. 2015. “Oncogenetic Testing, Diagnosis and Follow-up in Birt-Hogg-Dubé Syndrome, Familial Atypical Multiple Mole Melanoma Syndrome and Neurofibromatosis 1 and 2.” KCE Report. Brussels, Belgium: Federaal Kenniscentrum voor de Gezondheidszorg (KCE).
Vancouver
1.
Robays J, Stordeur S, Hulstaert F, Baurain J-F, Brochez L, Caplanusi T, et al. Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2. Vol. 243, KCE Report. Brussels, Belgium: Federaal Kenniscentrum voor de Gezondheidszorg (KCE); 2015.
IEEE
[1]
J. Robays et al., “Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2,” KCE Report, vol. 243. Federaal Kenniscentrum voor de Gezondheidszorg (KCE), Brussels, Belgium, 2015.
@misc{7221288,
  author       = {Robays, Jo and Stordeur, Sabine and Hulstaert, Frank and Baurain, Jean-François and Brochez, Lieve and Caplanusi, Teofila and Claes, Kathleen and Legius, Eric and Rottey, Sylvie and Schrijvers, Dirk and 't Kint de Roodenbeke, Daphné and Ullman, Urielle and Van Maerken, Tom and Poppe, Bruce},
  language     = {eng},
  pages        = {47},
  publisher    = {Federaal Kenniscentrum voor de Gezondheidszorg (KCE)},
  series       = {KCE Report},
  title        = {Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2},
  url          = {https://kce.fgov.be/publication/report/oncogenetic-testing-diagnosis-and-follow-up-in-birt-hogg-dub%C3%A9-syndrome-familial-a},
  volume       = {243},
  year         = {2015},
}