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BMC Pediatrics|March 1, 2018
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case reportJaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C Elalaoui, et al.
Acta Oto-Laryngologica|March 27, 2026
Genetic epidemiology of Moroccan pediatric cochlear implantation patientsEl Mostafa Salman, Omar Oulghoul, Mohammed Chehbouni, et al.
BMC Pediatrics|April 19, 2018
Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case reportJaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C Elalaoui, et al.
European Journal of Human Genetics : EJHG|March 16, 2017
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden deathNajim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, et al.
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