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BMC Medical Genetics|May 5, 2017
A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case reportW Smaili, S Chafai Elalaoui, S Meier, 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.Singapore Medical Journal|April 2, 2010
Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 casesI C Jaouad, S Cherkaoui Deqaqi, A Sbiti, et al.BMC Pediatrics|June 6, 2018
Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case reportH Berrani, T Meskini, M Zerkaoui, et al.Journal of Biosocial Science|May 13, 2009
Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disordersI Cherkaoui Jaouad, S Chafaï Elalaoui, A Sbiti, et al.Annales De Genetique|January 1, 1993
Isolation and characterisation of five new anonymous X-specific probes. One of them detecting a TaqI RFLPN Belhadj-Kacem, S Heuertz, M C Hors-Cayla, et al.Annales De Genetique|January 1, 1989
Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocationsA Sefiani, S Heuertz, C Turleau, et al.Indian Journal of Pediatrics|November 18, 2008
Omenn syndrome with mutation in RAG1 geneI Cherkaoui Jaouad, K Ouldim, S Ali Ou Alla, et al.European Journal of Medical Genetics|May 29, 2013
Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan familyI Cherkaoui Jaouad, M El Alloussi, F Z Laarabi, et al.Current Research in Translational Medicine|March 26, 2017
CALR gene mutational profile in myeloproliferative neoplasms with non-mutated JAK2 in Moroccan patients: A case series and germline in-frame deletionW Smaili, Y Doubaj, F Z Laarabi, et al.Pageof 5