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1. Predicting the impact of rare variants on RNA splicing in CAGI6

4. Predicting the impact of rare variants on RNA splicing in CAGI6

5. Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature

7. Short amplicon reverse transcription‐polymerase chain reaction detects aberrant splicing in genes with low expression in blood missed by ribonucleic acid sequencing analysis for clinical diagnosis

9. Comparison of in Silico Strategies to Prioritize Rare Genomic Variants Impacting RNA Splicing for the Diagnosis of Genomic Disorders

10. Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

11. Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders

12. Correction: Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

13. Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance

14. Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders

17. The Development and Growth of Tissues Derived from Cranial Neural Crest and Primitive Mesoderm Is Dependent on the Ligation Status of Retinoic Acid Receptor γ: Evidence That Retinoic Acid Receptor γ Functions to Maintain Stem/Progenitor Cells in the Absence of Retinoic Acid

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