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 |
Phenotype Variability in Progranulin Mutation Carriers: A Clinical, Neuropsychological, Imaging and Genetic Study |
Brain. , 131(Pt 3):732-46 |
|
2008 |
Fetal Presentation of Silver Russell Syndrome |
European Journal of Human Genetics |
|
2011 |
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 |
CHMP2B Mutations are Rare in French Families with Frontotemporal Lobar Degeneration. |
J Neurol, 257:2032–2036 |
|
2010 |