Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services

por Noor, Sahar, Hakimzada, Nasrin, Safi, Nijatullah, Alikozai, Sultan Mahmood, Rasooli, Abdul Jamil, Jalalzai, Tooryalai, Siddiqui, Qais, Sestani, Ahmad Jalil, Nasir, Najla, Noor, Sarah, Haidary, Ahmed Maseh, Khalid, Saifullah
Publicado 2023

Rare additional chromosomal abnormalities in acute promyelocytic leukaemia resulting in rapidly fatal disease: report of a case

por Haidary, Ahmed Maseh, Noor, Sarah, Noor, Sahar, Ahmad, Maryam, Yousufzai, Ahmad Walid, Saadaat, Ramin, Ahmed, Zeeshan Ansar, Rasooli, Abdul Jamil, Zahier, Ahmad Shekib, Malakzai, Haider Ali, Ibrahimkhil, Abdul Sami, Sharif, Samuel, Anwari, Mohammad Sarwar, Saqib, Abdul Hadi, Baryali, Tawab, Nasir, Najla
Publicado 2021