APA

Nallathambi J., Moumné L., De Baere E., Beysen D., Usha K., Sundaresan P. & Veitia R. A. (20070928). A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. : Human genetics.

Chicago

Nallathambi Jeyabalan, Moumné Lara, De Baere Elfride, Beysen Diane, Usha Kim, Sundaresan Periasamy and Veitia Reiner A. 20070928. A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. : Human genetics.

Harvard

Nallathambi J., Moumné L., De Baere E., Beysen D., Usha K., Sundaresan P. and Veitia R. A. (20070928). A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. : Human genetics.

MLA

Nallathambi Jeyabalan, Moumné Lara, De Baere Elfride, Beysen Diane, Usha Kim, Sundaresan Periasamy and Veitia Reiner A. A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. : Human genetics. 20070928.