10 results on '"Eid, Ola M."'
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2. Hot Spots Copy Number Variations, 15q Methylation, and SHANK3 Single Nucleotide Polymorphisms Sudy in a Group of Egyptian Autistic Children.
3. Cytogenetic and Clinical Description of Maternally Inherited Pure Trisomy 4p.
4. Phelan-McDermid Syndrome: Expanding the Phenotype.
5. Molecular characterization of patients with clinical suspicion of 22q11.2 deletion syndrome.
6. Cytogenetics abnormalities in a referred population for chromosomal analysis and the role of fluorescence in-situ hybridization in refining the diagnosis.
7. Molecular cytogenetic techniques for identification of copy-number variations.
8. Evaluation of the frequency of sister chromatid exchanges and micronuclei in children with type-1 diabetes mellitus.
9. Epilepsy and autistic manifestations in an Egyptian child with ring 14.
10. Cytokinesis-blocked micronucleus assay in a group of Egyptian patients with Fanconi anemia.
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