Faten Moassass

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

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Author's articles:

A NOVEL HETEROZYGOUS VARIANT IN EXON 32 OF THE CHD7 GENE (C.6923C>T) IN A SYRIAN FAMILY WITH KALLMANN SYNDROME
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Background: Kallmann syndrome (KS) and CHARGE syndrome (CS) are rare heritable disorders in which anosmia and hypogonadotropic hypogonadism ...
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Research Results in Biomedicine (ISSN 2658-6533)

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