Author Information
| Title | Journal Title, Volume, Page | Full Text |
Year of Publication |
|---|---|---|---|
| Assessment of Research Productivity of Arab Countries in the Field of Infectious Diseases using Web of Science Database | Infectious Diseases of Poverty, 4:2 | 2015 | |
| Possible Association Between Complex Congenital Heart Defects and 11p15 Hypomethylation in Three Patients with Severe Silver–Russell Syndrome | American Journal of Medical Genetics Part A Volume 161, Issue 3, pages 572–577 | 2013 | |
| Fetal Presentation of Silver Russell Syndrome | European Journal of Human Genetics | 2011 | |
| CHMP2B Mutations are Rare in French Families with Frontotemporal Lobar Degeneration. | J Neurol, 257:2032–2036 | 2010 | |
| Phenotype Variability in Progranulin Mutation Carriers: A Clinical, Neuropsychological, Imaging and Genetic Study | Brain. , 131(Pt 3):732-46 | 2008 |
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