HA
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders | Genome research |  | 2015 | 465 | 2 | ||
| Familial epilepsy in Algeria: Clinical features and inheritance profiles | Seizure | | 2015 | 518 | 0 | ||
| Recessive thrombocytopenia likely due to a homozygous pathogenic variant in the FYB gene: case report | BMC medical genetics |  | 2014 | 521 | 179 |
