Alfadhel, M., Alhubayshi, B. S., Umair, M., Alfaidi, A., Alwadaani, D., Aloyouni, E., . . . Al-Khenaizan, S. Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome). Sociedade Brasileira de Genética.
Chicago Style (17th ed.) CitationAlfadhel, Majid, et al. Truncated SPAG9 as a Novel Candidate Gene for a New Syndrome: Coarse Facial Features, Albinism, Cataract and Developmental Delay (CACD Syndrome). Sociedade Brasileira de Genética.
MLA (9th ed.) CitationAlfadhel, Majid, et al. Truncated SPAG9 as a Novel Candidate Gene for a New Syndrome: Coarse Facial Features, Albinism, Cataract and Developmental Delay (CACD Syndrome). Sociedade Brasileira de Genética.
Warning: These citations may not always be 100% accurate.