Your search returned 2 results.

Results
	1.	A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy. [electronic resource] by Alqahtani, Mohammad A Shati, Ayed A Zou, Minjing Alsuheel, Ali M Alhayani, Abdullah A Al-Qahtani, Saleh M Gilban, Hessa M Meyer, Brain F Shi, Yufei Producer: 20150812 In: International journal of endocrinology vol. 2015 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity. [electronic resource] by Al-Hassnan, Zuhair N Al-Fayyadh, Majid Al-Ghamdi, Bander Shafquat, Azam Mallawi, Yaseen Al-Hadeq, Faten Tulbah, Sahar Shinwari, Zarghuna M A Almesned, Abdulrahman Alakhfash, Ali Al Fadly, Fadel Hersi, Ahmed S Alhayani, Abdullah Al-Hashem, Amal Arafah, Dia Dzimiri, Nduna Meyer, Brian Rababh, Monther Al-Manea, Waleed Producer: 20180423 In: Heart rhythm vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search