1. A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype–phenotype nonconcordance. Issue 1 (20th August 2015) Authors: Khattab, Ahmed; Yuen, Tony; Al‐Malki, Sultan; Yau, Mabel; Kazmi, Diya; Sun, Li; Harbison, Madeleine; Haider, Shozeb; Zaidi, Mone; New, Maria I. Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1364:Issue 1(2016) Page Start: 5 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗