Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

MLA

Lacombe Didier, et al. “Complete Exon Sequencing of All Known Usher Syndrome Genes Greatly Improves Molecular Diagnosis.” Orphanet Journal of Rare Diseases, vol. 6, no. 1, May 2011, p. 21. EBSCOhost, https://doi.org/10.1186/1750-1172-6-21.

APA

Lacombe Didier, Mom Thierry, Francannet Christine, Duvillard Alain, Thauvin Christel, Dubin Jacques, Bonneau Dominique, Montaut-Verient Bettina, Vigneron Jacqueline, Calais Catherine, David Albert, Eliot Marie-Madeleine, Dollfus Hélène, Vincent Christophe, Delobel Bruno, Weil Dominique, El-Amraoui Aziz, Jonard Laurence, Feldmann Delphine, … Denoyelle Françoise. (2011). Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet Journal of Rare Diseases, 6(1), 21. https://doi.org/10.1186/1750-1172-6-21

Chicago

Lacombe Didier, Mom Thierry, Francannet Christine, Duvillard Alain, Thauvin Christel, Dubin Jacques, Bonneau Dominique, et al. 2011. “Complete Exon Sequencing of All Known Usher Syndrome Genes Greatly Improves Molecular Diagnosis.” Orphanet Journal of Rare Diseases 6 (1): 21. doi:10.1186/1750-1172-6-21.