Identification of a novel WFS1 homozygous nonsense mutation in Jordanian children with Wolfram syndrome

por Bodoor, Khaldon, Batiha, Osama, Abu-Awad, Ayman, Al-Sarihin, Khaldon, Ziad, Haya, Jarun, Yousef, Abu-sheikha, Aya, Abu Jalboush, Sara, Alibrahim, Khoulod S.
Publicado 2016

Berardinelli-Seip Syndrome and Essential Thrombocytosis: An Unusual Association

por Alzu’bi, Ali A., Al-Sarihin, Khaldon K., Eteiwi, Suzan, Al-Asaad, Rania A., Al Eyadah, Abdallah A., Khreisat, Maysa, Al-Omari, Ahmad A., Haddad, Fares H.
Publicado 2020