16 results on '"Fee, Timothy"'
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2. Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing
3. P549: Analysis of challenging products of conception cases with optical genome mapping: A preliminary study
4. P435: Diagnostic yield and copy number findings from 500 clinical genome sequencing cases
5. 7. Optical genome mapping for prenatal diagnostic testing
6. 18. Trisomy 18p detected in DNA from saliva but absent in DNA from blood
7. eP326: Genome sequencing reveals BHLHA9 gene duplication as cause of multi-generational split-hand/foot malformation with long bone deficiency
8. 52. Optical genome mapping and SNP microarray: integrated workflow for optimizing analysis of products of conception
9. 13. Next-generation cytogenetics: Proposal for a cost-effective approach for comprehensive testing of prenatal cases
10. Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
11. 23. Incidental findings on XON array: Our experience over the last two years
12. 17. In silico SNP array for aiding in interpretation of genomic microarray results: Application to case of mosaic trisomy 9
13. 47. Serendipitous identification of meiotic crossover events in struma ovarii tumors by whole genome SNP microarray analysis
14. 36. Identification and characterization of complete and partial MEF2C gene deletions in 3 individuals with developmental delay by whole genome microarray analysis
15. A bio-inspired hybrid nanosack for graft vascularization at the omentum
16. A simple device for closure of fasciotomy wounds
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