Cita APA

Deeb, A., Al Suwaidi, H., Attia, S., & Al Ameri, A. (2015). 17-hydroxylase/17,20-lyase deficiency due to a R96Q mutation causing hypertension and poor breast development. Endocrinol Diabetes Metab Case Rep.

Citación estilo Chicago

Deeb, Asma, Hana Al Suwaidi, Salima Attia, y Ahlam Al Ameri. "17-hydroxylase/17,20-lyase Deficiency Due to a R96Q Mutation Causing Hypertension and Poor Breast Development." Endocrinol Diabetes Metab Case Rep 2015.

Cita MLA

Deeb, Asma, Hana Al Suwaidi, Salima Attia, y Ahlam Al Ameri. "17-hydroxylase/17,20-lyase Deficiency Due to a R96Q Mutation Causing Hypertension and Poor Breast Development." Endocrinol Diabetes Metab Case Rep 2015.