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You searched for: Author/Creator Başaran, Seher

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1. Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey. (December 2021)

2. Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey. Issue 2 (17th November 2022)

3. Functional loss of ubiquitin‐specific protease 14 may lead to a novel distal arthrogryposis phenotype. Issue 4 (31st January 2022)

4. Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene. Issue 181 (July 2018)