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Abdullah Fahad Al-Mutery
Abdullah Fahad Al-Mutery
University of Sharjah
Biology
Endocrinology
Congenital Hypogonadotropic Hypogonadism
Internal medicine
NonStop
3
Papers
6
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0
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Mitochondrial mutations in non-syndromic hearing loss at UAE
2020
International Journal of Pediatric Otorhinolaryngology
Walaa Kamal Eldin Mohamed
Marc Arnoux
Thyago Hermylly Santana Cardoso
Abdullah Fahad Al-Mutery
Abdelaziz Tlili
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Séquençage à haut débit de l’exome entier d’une famille Tunisienne atteinte d’Hypogonadisme Hypogonadotrope Congénital Normosmique
2020
Annales D Endocrinologie
M. Moalla
Wajdi Safi
Dorra Ghorbel
Abdullah Fahad Al-Mutery
Mona Mahfood
N. Mejdoub-Rekik
Mohamed Abid
Mouna Mnif Feki
F. Hadj Kacem
H. Hadj Kacem
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Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism
2019
Journal of Assisted Reproduction and Genetics
Mariam Moalla
Faten Hadj Kacem
Abdullah Fahad Al-Mutery
Mona Mahfood
Nabila Mejdoub-Rekik
Mohamed Abid
Mouna Mnif Feki
Hassen Hadj Kacem
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Citations (5)
1