Faten Moassass
BS, MS, Researcher of Human Genetics Division, Molecular Biology and Biotechnology Department of the Atomic Energy Commission of Syria, ORCID: 0000-0002-4495-1866
Статьи автора:
Background: Kallmann syndrome (KS) and CHARGE syndrome (CS) are rare heritable disorders in which anosmia and hypogonadotropic hypogonadism ...