APA
Gueneau L., Duplomb L., Sarda P., Hamel C., Aral B., Chehadeh S. E., Gigot N., St-Onge J., Callier P., Thevenon J., Huet F., Carmignac V., Droin N., Faivre L. & Thauvin-Robinet C. (20140911). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. : American journal of medical genetics. Part A.
Chicago
Gueneau Lucie, Duplomb Laurence, Sarda Pierre, Hamel Christian, Aral Bernard, Chehadeh Salima El, Gigot Nadège, St-Onge Judith, Callier Patrick, Thevenon Julien, Huet Frédéric, Carmignac Virginie, Droin Nathalie, Faivre Laurence and Thauvin-Robinet Christel. 20140911. Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. : American journal of medical genetics. Part A.
Harvard
Gueneau L., Duplomb L., Sarda P., Hamel C., Aral B., Chehadeh S. E., Gigot N., St-Onge J., Callier P., Thevenon J., Huet F., Carmignac V., Droin N., Faivre L. and Thauvin-Robinet C. (20140911). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. : American journal of medical genetics. Part A.
MLA
Gueneau Lucie, Duplomb Laurence, Sarda Pierre, Hamel Christian, Aral Bernard, Chehadeh Salima El, Gigot Nadège, St-Onge Judith, Callier Patrick, Thevenon Julien, Huet Frédéric, Carmignac Virginie, Droin Nathalie, Faivre Laurence and Thauvin-Robinet Christel. Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. : American journal of medical genetics. Part A. 20140911.