APA

Abid F., Tardy V., Gaouzi A., El Hessni A., Morel Y. & Chabraoui L. (20090324). CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. : Clinical chemistry and laboratory medicine.

Chicago

Abid Fatima, Tardy Véronique, Gaouzi Ahmed, El Hessni Aboubaker, Morel Yves and Chabraoui Layachi. 20090324. CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. : Clinical chemistry and laboratory medicine.

Harvard

Abid F., Tardy V., Gaouzi A., El Hessni A., Morel Y. and Chabraoui L. (20090324). CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. : Clinical chemistry and laboratory medicine.

MLA

Abid Fatima, Tardy Véronique, Gaouzi Ahmed, El Hessni Aboubaker, Morel Yves and Chabraoui Layachi. CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation. : Clinical chemistry and laboratory medicine. 20090324.