Nour A L Fakseh

发表

A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family

Hossam Murad, Faten Moassas, Nour A L Fakseh, 2021, Molecular genetics & genomic medicine.