11 results on '"Yesil, Gozde"'
Search Results
2. Biallelic loss of TRAPPC9 function links vesicle trafficking pathway to autosomal recessive intellectual disability
3. Evaluation of the parents’ anxiety levels before and after the diagnosis of their child with a rare genetic disease: the necessity of psychological support
4. A rare cause of hypertension in childhood: Answers
5. A rare cause of hypertension in childhood: Questions
6. Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers
7. Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions
8. Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature
9. Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey
10. The Effect of Genetic Polymorphisms of Cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on Drug-Resistant Epilepsy in Turkish Children
11. The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.