31 results on '"Koleilat, Alaa"'
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2. Disparity in the detection of chromosome 15 centromere in patients of African ancestry with a plasma cell neoplasm
3. Concurrent TERT promoter C228T and C250T mutations in diffuse gliomas: Rare occurrence of intratumoral heterogeneity
4. The Importance of Mitochondrial Disease Testing in Young Adults With New Onset Sensorineural Hearing Loss.
5. Confirmation of Insertion, Deletion, and Deletion-Insertion Variants Detected by Next-Generation Sequencing
6. Chapter 20 - Hearing loss
7. Three-Dimensional Structure of Inner Ear Hair Cell Ribbon Synapses in a Zebrafish Model of Usher Syndrome Type 1B
8. P688: A pilot mentorship program for the career advancement of underrepresented individuals in laboratory genomics at Mayo Clinic
9. P496: The importance of mitochondrial disease testing in young adults with new onset sensorineural hearing loss
10. Concurrent TERTpromoter C228T and C250T mutations in diffuse gliomas: Rare occurrence of intratumoral heterogeneity
11. 90. TERT promoter mutation detection by ddPCR in glial atypia
12. 49. Reduced performance of centromere 15 probe in association with African ancestry
13. Three-dimensional structure of inner ear hair cell mitochondrial networks and ribbon synapses in a zebrafish model of Usher syndrome type 1B
14. Characterization of unusual iAMP21 B‐lymphoblastic leukemia ( iAMP21‐ALL ) from the Mayo Clinic and Children's Oncology Group
15. OP038: Novel whole methylome automated data analysis tool for investigation of unsolved diagnostic odyssey cases
16. 22. Characterization of atypical iAMP21 observed in B-Lymphoblastic Leukemia (B-ALL): A retrospective study from Mayo Clinic
17. Contributors
18. False-Negative Centromere 15 Probe Results in Association with African Ancestry in Plasma Cell Dyscrasias
19. Utilizing next-generation sequencing to characterize a case of acute myeloid leukemia with t(4;12)(q12;p13) in the absence of ETV6/CHIC2 and ETV6/PDGFRA gene fusions
20. New Tmc1 Deafness Mutations Impact Mechanotransduction in Auditory Hair Cells
21. 30. Characterization of atypical iAMP21 observed in B-Lymphoblastic Leukemia (B-ALL): a 2.5-year retrospective study from the Mayo Clinic
22. The GoAudio Quantitative Mobile Audiology Test Enhances Access to Clinical Hearing Assessments
23. L-type voltage-gated calcium channel agonists mitigate hearing loss and modify ribbon synapse morphology in the zebrafish model of Usher syndrome type 1
24. Emerging Therapies and Approaches to Treat and Prevent Hearing Loss
25. Utilizing next-generation sequencing to characterize a case of acute myeloid leukemia with t(4;12)(q12;p13) in the absence of ETV6/CHIC2 and ETV6/PDGFRA gene fusions.
26. Current Approaches to the Management of Usher Syndrome for the Clinician
27. L-type voltage-gated calcium channel agonists improve hearing loss and modify ribbon synapse morphology in the zebrafish model of Usher Syndrome Type 1
28. Modeling SLC26A4 Associated Hearing Loss Using Zebrafish as a Model System
29. Allele-Specific Quantitative PCR for Accurate, Rapid, and Cost-Effective Genotyping
30. Laparoscopic Vertical Sleeve Gastrectomy for the Treatment of Pseudotumor Cerebri
31. SLEEVE GASTRECTOMY FAILURE: Just When We Thought We Had the Perfect Operation.
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