13 results on '"Dincer, Yasemin"'
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2. Monogenic variants in dystonia: an exome-wide sequencing study
3. De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy
4. Recessive NUP54 Variants Underlie Early‐Onset Dystonia with Striatal Lesions
5. Recessive NUP54 Variants Underlie Early‐Onset Dystonia with Striatal Lesions.
6. Clinically relevant copy-number variants in exome sequencing data of patients with dystonia
7. Clinical, neuroimaging, and molecular spectrum of TECPR2 ‐associated hereditary sensory and autonomic neuropathy with intellectual disability
8. De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy
9. Clinical, neuroimaging and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability
10. FV 1031. Whole Exome Sequencing for Children with Dyskinetic Movement Disorder
11. Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations
12. Increased PDGFR-beta and VEGFR-2 protein levels are associated with resistance to platinum-based chemotherapy and adverse outcome of ovarian cancer patients
13. Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations.
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