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American Journal of Medical Genetics. Part A|May 14, 2011
GM2 gangliosidosis in Saudi Arabia: multiple mutations and considerations for future carrier screeningNamik Kaya, Mohammad Al-Owain, Nada Abudheim, et al.Molecular Cancer|June 15, 2010
Integrative and comparative genomics analysis of early hepatocellular carcinoma differentiated from liver regeneration in young and oldDilek Colak, Muhammad A Chishti, Al-Bandary Al-Bakheet, et al.Molecular Cytogenetics|April 5, 2011
Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defectsJawaher Al-Zahrani, Naji Al-Dosari, Nada Abudheim, et al.Journal of Inherited Metabolic Disease|September 20, 2012
Clinical and biochemical features associated with BCS1L mutationMohammed Al-Owain, Dilek Colak, Albandary Albakheet, et al.Annals of Neurology|January 4, 2012
A novel X-linked disorder with developmental delay and autistic featuresNamik Kaya, Dilek Colak, Albandary Albakheet, et al.Pageof 2