| Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders | Genome research |  | | 2015 | 561 | 2 |
|
| Familial epilepsy in Algeria: Clinical features and inheritance profiles | Seizure | | | 2015 | 572 | 0 |
|
| Recessive thrombocytopenia likely due to a homozygous pathogenic variant in the FYB gene: case report | BMC medical genetics |  | | 2014 | 576 | 241 |
|
