APA
Gardie B., Remenieras A., Kattygnarath D., Bombled J., Lefèvre S., Perrier-Trudova V., Rustin P., Barrois M., Slama A., Avril M., Bessis D., Caron O., Caux F., Collignon P., Coupier I., Cremin C., Dollfus H., Dugast C., Escudier B., Faivre L., Field M., Gilbert-Dussardier B., Janin N., Leport Y., Leroux D., Lipsker D., Malthieu F., McGilliwray B., Maugard C., Méjean A., Mortemousque I., Plessis G., Poppe B., Pruvost-Balland C., Rooker S., Roume J., Soufir N., Steinraths M., Tan M., Théodore C., Thomas L., Vabres P., Van Glabeke E., Meric J., Verkarre V., Lenoir G., Joulin V., Deveaux S., Cusin V., Feunteun J., Teh B. T., Bressac-de Paillerets B. & Richard S. (20110729). Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. : Journal of medical genetics.
Chicago
Gardie Betty, Remenieras Audrey, Kattygnarath Darouna, Bombled Johny, Lefèvre Sandrine, Perrier-Trudova Victoria, Rustin Pierre, Barrois Michel, Slama Abdelhamid, Avril Marie-Françoise, Bessis Didier, Caron Olivier, Caux Frédéric, Collignon Patrick, Coupier Isabelle, Cremin Carol, Dollfus Hélène, Dugast Catherine, Escudier Bernard, Faivre Laurence, Field Michel, Gilbert-Dussardier Brigitte, Janin Nicolas, Leport Yves, Leroux Dominique, Lipsker Dan, Malthieu Félicia, McGilliwray Barbara, Maugard Christine, Méjean Arnaud, Mortemousque Isabelle, Plessis Ghislaine, Poppe Bruce, Pruvost-Balland Christelle, Rooker Serena, Roume Joelle, Soufir Nadem, Steinraths Michelle, Tan Min-Han, Théodore Christine, Thomas Luc, Vabres Pierre, Van Glabeke Emmanuel, Meric Jean-Baptiste, Verkarre Virginie, Lenoir Gilbert, Joulin Virginie, Deveaux Sophie, Cusin Veronica, Feunteun Jean, Teh Bin Tean, Bressac-de Paillerets Brigitte and Richard Stéphane. 20110729. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. : Journal of medical genetics.
Harvard
Gardie B., Remenieras A., Kattygnarath D., Bombled J., Lefèvre S., Perrier-Trudova V., Rustin P., Barrois M., Slama A., Avril M., Bessis D., Caron O., Caux F., Collignon P., Coupier I., Cremin C., Dollfus H., Dugast C., Escudier B., Faivre L., Field M., Gilbert-Dussardier B., Janin N., Leport Y., Leroux D., Lipsker D., Malthieu F., McGilliwray B., Maugard C., Méjean A., Mortemousque I., Plessis G., Poppe B., Pruvost-Balland C., Rooker S., Roume J., Soufir N., Steinraths M., Tan M., Théodore C., Thomas L., Vabres P., Van Glabeke E., Meric J., Verkarre V., Lenoir G., Joulin V., Deveaux S., Cusin V., Feunteun J., Teh B. T., Bressac-de Paillerets B. and Richard S. (20110729). Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. : Journal of medical genetics.
MLA
Gardie Betty, Remenieras Audrey, Kattygnarath Darouna, Bombled Johny, Lefèvre Sandrine, Perrier-Trudova Victoria, Rustin Pierre, Barrois Michel, Slama Abdelhamid, Avril Marie-Françoise, Bessis Didier, Caron Olivier, Caux Frédéric, Collignon Patrick, Coupier Isabelle, Cremin Carol, Dollfus Hélène, Dugast Catherine, Escudier Bernard, Faivre Laurence, Field Michel, Gilbert-Dussardier Brigitte, Janin Nicolas, Leport Yves, Leroux Dominique, Lipsker Dan, Malthieu Félicia, McGilliwray Barbara, Maugard Christine, Méjean Arnaud, Mortemousque Isabelle, Plessis Ghislaine, Poppe Bruce, Pruvost-Balland Christelle, Rooker Serena, Roume Joelle, Soufir Nadem, Steinraths Michelle, Tan Min-Han, Théodore Christine, Thomas Luc, Vabres Pierre, Van Glabeke Emmanuel, Meric Jean-Baptiste, Verkarre Virginie, Lenoir Gilbert, Joulin Virginie, Deveaux Sophie, Cusin Veronica, Feunteun Jean, Teh Bin Tean, Bressac-de Paillerets Brigitte and Richard Stéphane. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. : Journal of medical genetics. 20110729.