APA

Savastano C. P., Brito L. A., Faria Á. C., Setó-Salvia N., Peskett E., Musso C. M., Alvizi L., Ezquina S. A. M., James C., Beales P., Lees M., Moore G. E., Stanier P. & Passos-Bueno M. R. (20170602). Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. : Clinical genetics.

Chicago

Savastano C P, Brito L A, Faria Á C, Setó-Salvia N, Peskett E, Musso C M, Alvizi L, Ezquina S A M, James C, Beales P, Lees M, Moore G E, Stanier P and Passos-Bueno M R. 20170602. Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. : Clinical genetics.

Harvard

Savastano C. P., Brito L. A., Faria Á. C., Setó-Salvia N., Peskett E., Musso C. M., Alvizi L., Ezquina S. A. M., James C., Beales P., Lees M., Moore G. E., Stanier P. and Passos-Bueno M. R. (20170602). Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. : Clinical genetics.

MLA

Savastano C P, Brito L A, Faria Á C, Setó-Salvia N, Peskett E, Musso C M, Alvizi L, Ezquina S A M, James C, Beales P, Lees M, Moore G E, Stanier P and Passos-Bueno M R. Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. : Clinical genetics. 20170602.