10 results on '"Hadzsiev, Kinga"'
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2. Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate
3. Expanded phenotype of AARS1-related white matter disease
4. Rubinstein–Taybi syndrome 2 with cerebellar abnormality and neural tube defect
5. A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics
6. Cytochrome P450 Drug Metabolizing Enzymes in Roma Population Samples: Systematic Review of the Literature
7. Increased prevalence of functional minor allele variants of drug metabolizing CYP2B6 and CYP2D6 genes in Roma population samples
8. Phenotypic Variants of the Deafness-Associated Mitochondrial DNA A7445G Mutation
9. Excess of malignancies in grandparents of children with malformations?
10. Mutation analysis of MECP2 and determination of the X‐inactivation pattern in Hungarian Rett syndrome patients
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