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Journal of Pediatric Genetics|February 19, 2019
A Novel De Novo Frameshift Mutation in KAT6A Identified by Whole Exome SequencingAsem Alkhateeb, Wafa AlazaizehArchives of Dermatological Research|June 25, 2010
Genetic association of NALP1 with generalized vitiligo in Jordanian ArabsAsem Alkhateeb, Firas QarqazAutoimmunity|February 5, 2013
Polymorphisms in NLRP1 gene and susceptibility to autoimmune thyroid diseaseAsem Alkhateeb, Yousef Jarun, Reema TashtoushDisease Markers|October 14, 2009
Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same regionAsem Alkhateeb, Amal Uzrail, Khaldon BodoorEuropean Journal of Dermatology : EJD|October 23, 2010
SMOC2 gene variant and the risk of vitiligo in Jordanian ArabsAsem Alkhateeb, Nour Al-Dain Marzouka, Firas QarqazEndocrine|March 7, 2013
Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab populationAsem Alkhateeb, Nour Al-Dain Marzouka, Reema TashtoushGene|October 9, 2012
Genetic association of adiponectin with type 2 diabetes in Jordanian Arab populationAsem Alkhateeb, Sayer Al-Azzam, Raya Zyadine, et al.Human Mutation|May 15, 2002
Propionic acidemia: analysis of mutant propionyl-CoA carboxylase enzymes expressed in Escherichia coliMaja Chloupkova, Kenneth N Maclean, Asem Alkhateeb, et al.Molecular Diagnosis & Therapy|June 22, 2010
Clinical characteristics and PTPN22 1858C/T variant analysis in Jordanian Arab vitiligo patientsAsem Alkhateeb, Firas Qarqaz, Jude Al-Sabah, et al.Journal of Biomedical Informatics|November 15, 2011
Protein contact map prediction using multi-stage hybrid intelligence inference systemsAnas A Abu-Doleh, Omar M Al-Jarrah, Asem AlkhateebPageof 3