41 results on '"Booker, Jessica K."'
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2. Common-variant associations with fragile X syndrome
3. Chapter 39 - Molecular testing in the assessment of bone marrow transplant engraftment
4. Correction: Common-variant associations with fragile X syndrome
5. Monitoring Engraftment of Bone Marrow Transplant by DNA Fingerprinting
6. List of Contributors
7. Molecular Assessment of Bone Marrow Transplant Engraftment
8. CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids
9. List of contributors
10. Validation of Clinical Testing for Warfarin Sensitivity: Comparison of CYP2C9-VKORC1 Genotyping Assays and Warfarin-Dosing Algorithms
11. Detection of Common Disease-Causing Mutations in Mitochondrial DNA (Mitochondrial Encephalomyopathy, Lactic Acidosis with Stroke-Like Episodes MTTL1 3243 A>G and Myoclonic Epilepsy Associated with Ragged-Red Fibers MTTK 8344A>G) by Real-Time Polymerase Chain Reaction
12. Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project
13. Sensorineural Hearing Loss in a Pediatric Population: Association of Congenital Cytomegalovirus Infection With Intracranial Abnormalities
14. Molecular Assessment of Bone Marrow Transplant Engraftment
15. False-Negative Factor V Leiden Genetic Testing in a Patient With Recurrent Deep Venous Thrombosis
16. Mosaicism for an FMR1 gene deletion in a fragile X female
17. Correction: Common-variant associations with fragile X syndrome
18. Common-variant associations with fragile X syndrome
19. Fine-Needle Aspiration Smears as a Potential Source of DNA for Targeted Next-generation Sequencing of Lung Adenocarcinomas
20. Common Variant Associations with Fragile X Syndrome
21. Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing
22. CSF1Rmosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids
23. A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
24. FNA smears as a potential source of DNA for targeted next‐generation sequencing of lung adenocarcinomas
25. +ACA BRCA1 promoter polymorphism genotypic frequency among unaffected individuals and breast disease patients
26. High levels of Epstein–Barr virus DNA in latently infected gastric adenocarcinoma
27. +ACA BRCA1 promoter polymorphism confers increased risk of breast cancer among African‐American women
28. Increased Uptake of BRCA1/2 Genetic Testing Among African American Women With a Recent Diagnosis of Breast Cancer
29. A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort
30. Glutaric acidemia type 1 in patients of Lumbee heritage from North Carolina
31. Molecular Assessment of Bone Marrow Transplant Engraftment.
32. Expression and Function of Fas on Cells Damaged by γ-Irradiation in B6 and B6/lpr Mice
33. Clinical Applications of PCR (Methods in Molecular Medicine, Volume 16).
34. Mechanisms that limit the diversity of antibodies. II. Evolutionary conservation of Ig variable region genes which encode naturally occurring autoantibodies
35. Characterization of Expanded Populations of Peritoneal CD5 B Cells Specific for Phosphatidyl Choline in Old B10.H‐2aH‐4bp/Wts Micea
36. Characterization of Expanded Populations of Peritoneal CD5 B Cells Specific for Phosphatidyl Choline in Old B10.H-2aH-4bp/Wts Micea.
37. Detection of Common Disease-Causing Mutations in Mitochondrial DNA (Mitochondrial Encephalomyopathy, Lactic Acidosis with Stroke-Like Episodes MTTL13243 AG and Myoclonic Epilepsy Associated with Ragged-Red Fibers MTTK8344AG) by Real-Time Polymerase Chain Reaction
38. High levels of Epstein–Barr virus DNA in latently infected gastric adenocarcinoma
39. A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
40. Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalities.
41. The Prothrombin 20209C>T Sequence Variant: To Test or Not to Test.
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