Dergiler / Turkish Journal of Hematology / 2020 / Cilt: 37 - Sayı: 4
Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation
- Sayfa
- 296–298
- DOI
- —
Dergiler / Turkish Journal of Hematology / 2020 / Cilt: 37 - Sayı: 4