7 results on '"Yesil, Gozde"'
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2. Homozygous Loss-of-function Mutations in SOHLH1 in Patients With Nonsyndromic Hypergonadotropic Hypogonadism
3. Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes
4. Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes
5. The Effect of Genetic Polymorphisms of Cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on Drug-Resistant Epilepsy in Turkish Children
6. Report of a patient with Temple–Baraitser syndrome
7. Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations
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