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Mohammad Ahmad Awwad Alqahtani
Mohammad Ahmad Awwad Alqahtani
Endocrinology
Internal medicine
Medicine
Congenital adrenal hyperplasia
Cardiomyopathy
3
Papers
37
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Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation is a Novel Defect in Thyroid Dyshormonogenesis.
2018
The Journal of Clinical Endocrinology and Metabolism
Minjing Zou
Ali S. Alzahrani
Ali Al-Odaib
Mohammad Ahmad Awwad Alqahtani
Omer Babiker
Roua A. Al-Rijjal
Huda BinEssa
Walaa E. Kattan
Anwar F. Alenezi
Ali Ahmed Al Qarni
Manar S. A. Al-Faham
Essa Y. Baitei
Afaf Alsagheir
Brian F. Meyer
Yufei Shi
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Citations (28)
Steroid 11[beta]-Hydroxylase Deficient Congenital Adrenal Hyperplasia with a Reversible Cardiomyopathy Caused by a Novel CYP11B1 Mutation: Report of Three Cases
2015
Mohammad Ahmad Awwad Alqahtani
Ayed A. Shati
Minjing Zou
Ali M. Alsuheel
Abdullah A. Alhayani
Saleh M. Al-Qahtani
Hessa M. Gilban
Brain F. Meyer
Yufei Shi
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A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy
2015
International Journal of Endocrinology
Mohammad Ahmad Awwad Alqahtani
Ayed A. Shati
Minjing Zou
Ali M. Alsuheel
Abdullah A. Alhayani
Saleh M. Al-Qahtani
Hessa M. Gilban
Brain F. Meyer
Yufei Shi
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Citations (9)
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