APA

Imbard A., Pasmant E., Sabbagh A., Luscan A., Soares M., Goussard P., Blanché H., Laurendeau I., Ferkal S., Vidaud M., Pinson S., Bellanne-Chantelot C., Vidaud D., Wolkenstein P. & Parfait B. (20151009). NF1 single and multi-exons copy number variations in neurofibromatosis type 1. : Journal of human genetics.

Chicago

Imbard Apolline, Pasmant Eric, Sabbagh Audrey, Luscan Armelle, Soares Magali, Goussard Philippe, Blanché Hélène, Laurendeau Ingrid, Ferkal Salah, Vidaud Michel, Pinson Stéphane, Bellanne-Chantelot Christine, Vidaud Dominique, Wolkenstein Pierre and Parfait Béatrice. 20151009. NF1 single and multi-exons copy number variations in neurofibromatosis type 1. : Journal of human genetics.

Harvard

Imbard A., Pasmant E., Sabbagh A., Luscan A., Soares M., Goussard P., Blanché H., Laurendeau I., Ferkal S., Vidaud M., Pinson S., Bellanne-Chantelot C., Vidaud D., Wolkenstein P. and Parfait B. (20151009). NF1 single and multi-exons copy number variations in neurofibromatosis type 1. : Journal of human genetics.

MLA

Imbard Apolline, Pasmant Eric, Sabbagh Audrey, Luscan Armelle, Soares Magali, Goussard Philippe, Blanché Hélène, Laurendeau Ingrid, Ferkal Salah, Vidaud Michel, Pinson Stéphane, Bellanne-Chantelot Christine, Vidaud Dominique, Wolkenstein Pierre and Parfait Béatrice. NF1 single and multi-exons copy number variations in neurofibromatosis type 1. : Journal of human genetics. 20151009.