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I Ratbi

Showing results (1-10 of 9) with videos related to

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Annales De Dermatologie Et De Venereologie|January 10, 2012
[Congenital lower lip pits]N Fejjal, I Ratbi, F Benabdellah
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.
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.
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.
BMC Pediatrics|November 15, 2015
Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case reportM Zerkaoui, I Ratbi, B Castellotti, et al.
Gene|January 24, 2012
Non-association of Crohn's disease with NOD2 gene variants in Moroccan patientsI Hama, I Ratbi, S Reggoug, et al.
Molecular Syndromology|May 9, 2013
Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 MutationI Ratbi, N Fejjal, L Micale, et al.
Journal of Medical Case Reports|April 3, 2017
Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case reportN Adadi, N Lahrouchi, R Bouhouch, et al.
Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case ReportA Lamzouri, A El Rherbi, I Ratbi, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Annales De Dermatologie Et De Venereologie|January 10, 2012
[Congenital lower lip pits]N Fejjal, I Ratbi, F Benabdellah
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.
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.
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.
BMC Pediatrics|November 15, 2015
Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case reportM Zerkaoui, I Ratbi, B Castellotti, et al.
Gene|January 24, 2012
Non-association of Crohn's disease with NOD2 gene variants in Moroccan patientsI Hama, I Ratbi, S Reggoug, et al.
Molecular Syndromology|May 9, 2013
Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 MutationI Ratbi, N Fejjal, L Micale, et al.
Journal of Medical Case Reports|April 3, 2017
Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case reportN Adadi, N Lahrouchi, R Bouhouch, et al.
Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case ReportA Lamzouri, A El Rherbi, I Ratbi, et al.
Pageof 1