82 results on '"Lai, Poh San"'
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2. Embryo and fetal gene editing: Technical challenges and progress toward clinical applications
3. Spinal Muscular Atrophy: Evaluation of New Emerging Methods for Carrier Screening and Diagnosis
4. A clinical approach to diagnosis and management of mitochondrial myopathies
5. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
6. PYCR1 Levels Track with Premature and Chronological Skin Aging
7. PYCR1 Levels Track with Premature and Chronological Skin Aging
8. PYCR1 Levels Track with Premature and Chronological Skin Aging
9. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
10. P220: A de novo Xq13.2-13.3 duplication associated with non-syndromic intellectual disability
11. Expanding the genetic causes of small‐fiber neuropathy:SCNgenes and beyond
12. J’Accuse….. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing
13. Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis
14. Vulnerability and the Ethics of Human Germline Genome Editing
15. Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
16. Novel Autoantibodies in Idiopathic Small Fiber Neuropathy
17. Ethical considerations of preconception and prenatal gene modification in the embryo and fetus
18. Germline genome modification through novel political, ethical, and social lenses
19. Genetic variation in the oxytocin system and its link to social motivation in human infants
20. Blending oxytocin and dopamine with everyday creativity
21. Modeling the Genetics of Social Cognition in the Laboratory
22. Effects of Mindfulness-Based Stress Reduction on Affect Dynamics: a Randomized Controlled Trial
23. Dried Blood Spot Screening System for Spinal Muscular Atrophy with Allele-Specific Polymerase Chain Reaction and Melting Peak Analysis
24. Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene
25. Effects of Mindfulness-Based Stress Reduction on Psychological Symptoms and Telomere Length: A Randomized Active-Controlled Trial
26. The orphan nuclear receptorNR0B2could be a novel susceptibility locus associated with microsatellite‐stable,APCmutation‐negative early‐onset colorectal carcinomas with metabolic manifestation
27. Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management
28. Design of Split Proximity Circuit as a Plug-and-Play Translator for Point Mutation Discrimination
29. Correction to: Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults
30. Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults
31. The Creative Mind: Blending Oxytocinergic, Dopaminergic and Personality
32. Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapy
33. Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia
34. Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing
35. Successful aging, cognitive function, socioeconomic status, and leukocyte telomere length
36. Training in clinical genetics and genetic counseling in Asia
37. Development of clinical genetics in Asia
38. The role of the Oxytocin-Neurophysin I gene in contributing to human personality traits promoting sociality
39. Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2
40. Genetic Variation in the Maternal Oxytocin System Affects Cortisol Responsiveness to Breastfeeding in Infants and Mothers
41. Malignant Hyperthermia and Ryanodine Receptor Type 1 Gene (RyR1) Mutation in a Family in Singapore
42. Spinal muscular atrophy carriers with two SMN1 copies
43. Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA
44. AB109. Novel constitutional and somatic RB1 mutations underlying retinal cancers in addition to TNFα, KIF13A and MGMT alterations
45. AB132. The role of oxytocin-neurophysin I in contributing to human personality traits and plasma immunogenic oxytocin levels
46. SMA mutations in SMN Tudor and C-terminal domains destabilize the protein
47. Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling
48. ADP ribosyl-cyclases ( CD38 / CD157 ), social skills and friendship
49. Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2
50. Delay discounting, genetic sensitivity, and leukocyte telomere length
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