Hasil Pencarian - Bouchaïb Gazzaz
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1
A novel variant of unknown significance in pediatric epilepsy: a case report oleh Wafaa Bouzroud, Amal Tazzite, Ikhlass Boussakri, Bouchaïb Gazzaz, Hind Dehbi
Diterbitkan 2023-07-01
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2
R306X Mutation in the Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report oleh Wafaa Bouzroud, Amal Tazzite, Sarah Berrada, Bouchaïb Gazzaz, Hind Dehbi
Diterbitkan 2022-09-01
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3
Complement Factor I deficiency: A novel homozygous gene mutation oleh Wafaa Bouzroud, Amal Tazzite, Ibenbrahim yousra, Bouchaïb Gazzaz, Hind Dehbi
Diterbitkan 2022-06-01
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4