Rousseau, G., Noguchi, T., Bourdon, V., Sobol, H., & Olschwang, S. (2011). SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis. BioMed Central.
Citação norma ChicagoRousseau, Guillaume, Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol, and Sylviane Olschwang. SMARCB1/INI1 Germline Mutations Contribute to 10% of Sporadic Schwannomatosis. BioMed Central, 2011.
ציטוט MLARousseau, Guillaume, et al. SMARCB1/INI1 Germline Mutations Contribute to 10% of Sporadic Schwannomatosis. BioMed Central, 2011.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.