Cite
Combining gene mapping and phenotype assessment for fast mutation finding in non consanguineous autosomal recessive retinitis pigmentosa
MLA
Hébrard, Maxime, et al. Combining Gene Mapping and Phenotype Assessment for Fast Mutation Finding in Non Consanguineous Autosomal Recessive Retinitis Pigmentosa. July 2011. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.od.......212..c4933163b25f259ecc03b9ebb4f4f3c6&authtype=sso&custid=ns315887.
APA
Hébrard, M., Bocquet, B., Meunier, I., Coustes-Chazalette, D., Hérald, E., Sénéchal, A., Bolland Augé, A., Zelenika, D., Manès, G., & Hamel, C. P. (2011). Combining gene mapping and phenotype assessment for fast mutation finding in non consanguineous autosomal recessive retinitis pigmentosa.
Chicago
Hébrard, Maxime, Béatrice Bocquet, Isabelle Meunier, Delphine Coustes-Chazalette, Emilie Hérald, Audrey Sénéchal, Anne Bolland Augé, Diana Zelenika, Gaël Manès, and Christian P Hamel. 2011. “Combining Gene Mapping and Phenotype Assessment for Fast Mutation Finding in Non Consanguineous Autosomal Recessive Retinitis Pigmentosa,” July. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.od.......212..c4933163b25f259ecc03b9ebb4f4f3c6&authtype=sso&custid=ns315887.