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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 2, 2011
[Spinal muscular atrophy: frequent cause of congenital hypotonia in Morocco]A Sbiti, I Ratbi, Y Kriouile, et al.Journal of Medical Genetics|December 24, 1998
Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan familyK Kabbaj, L Baala, H Chhoul, et al.Journal of the Neurological Sciences|August 1, 1996
Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosisB Moulard, A Sefiani, A Laamri, et al.European Journal of Medical Genetics|February 16, 2010
Autosomal dominant microtiaS Chafai Elalaoui, I Cherkaoui Jaouad, L Rifai, et al.Current Research in Translational Medicine|May 4, 2016
Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 geneL Boualla, W Jdioui, K Soulami, et al.Balkan Journal of Medical Genetics : BJMG|September 21, 2020
Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the <i>TP63</i> GeneM Tajir, J Lyahyai, S Guaoua, et al.Molecular Syndromology|February 20, 2014
Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann SyndromeS C Elalaoui, I Garin, A Sefiani, et al.Annals of Human Biology|October 14, 2010
Prevalence of MYH-associated polyposis related to three recurrent mutations in MoroccoF Z Laarabi, I Cherkaoui Jaouad, A Benazzouz, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 19, 2007
[The mutation 35delG of the gene of the connexin 26 is a frequent cause of autosomal-recessive non-syndromic hearing loss in Morocco]I Ratbi, S Hajji, K Ouldim, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 22, 2011
[Three cases of Hutchinson-Gilford progeria syndrome]Y Doubaj, A Lamzouri, S-C Elalaoui, et al.Pageof 5