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You searched for: Author/Creator Setoodeh, Aria

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1. Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion). Issue 4 (3rd February 2022)

2. Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Issue 6 (29th August 2018)

3. Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46, XY Disorders of Sex Development with normal testicular development. (27th February 2019)

4. P.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche. (15th May 2020)