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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|March 1, 2011
[Confirmation of the high prevalence in Morocco of the homozygous mutation c.144delC in the aurora kinase C gene (AURKC) in the teratozoospermia with large-headed spermatozoa]F El Kerch, A Lamzouri, F Z Laarabi, 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.Genomics|April 1, 1989
The gene for incontinentia pigmenti is assigned to Xq28A Sefiani, L Abel, S Heuertz, et al.Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.Journal Francais D'Ophtalmologie|January 9, 2010
[First North African observation of Leber congenital amaurosis secondary to CEP290 gene mutation]N Aboussair, A Berahou, I Perrault, 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.Gene|January 24, 2012
The first mutations in the MYH gene reported in Moroccan colon cancer patientsF Z Laarabi, I Cherkaoui Jaouad, S Baert-Desurmont, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|May 11, 2005
[Haemangioma of the right atrium revealed by cardiogenic shock]L Marmade, M Laaroussi, M Elkouache, et al.Journal Francais D'Ophtalmologie|November 6, 2007
[Incontinentia pigmenti: a case study]B Tnacheri Ouazzani, K Guedira, H Dali, et al.Pageof 5