Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects

Por Ganji, Hamid, Salehi, Mansoor, Sedghi, Maryam, Abdali, Hossein, Nouri, Nayereh, Sadri, Leyli, Hosseinzadeh, Majid, Vakili, Bahareh, Lotfi, Mahdi
Publicado no Heart Asia (2013)