A novel de novo nonsense mutation in SALL4 causing duane radial ray syndrome: a case report and expanding the phenotypic spectrum

por Ajam-Hosseini, Mobarakeh, Parvini, Farshid, Angaji, Abdolhamid
Publicado 2023

Role of CYP1A1, CYP2D6, and NOS3 gene polymorphisms in idiopathic recurrent pregnancy loss in the Iranian Azeri population: A case-control study

por Yousefian, Mahsa, Angaji, Abdolhamid, Siasi, Elham, Ali Rahmani, Seyed, Abbasalizadeh Khiaban, Shamsi
Publicado 2022