16 results on '"Lai, Poh San"'
Search Results
2. A clinical approach to diagnosis and management of mitochondrial myopathies
3. Genetic variation in the oxytocin system and its link to social motivation in human infants
4. Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene
5. Effects of Mindfulness-Based Stress Reduction on Psychological Symptoms and Telomere Length: A Randomized Active-Controlled Trial
6. Successful aging, cognitive function, socioeconomic status, and leukocyte telomere length
7. The role of the Oxytocin-Neurophysin I gene in contributing to human personality traits promoting sociality
8. Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2
9. Spinal muscular atrophy carriers with two SMN1 copies
10. Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA
11. SMA mutations in SMN Tudor and C-terminal domains destabilize the protein
12. ADP ribosyl-cyclases (CD38/CD157), social skills and friendship
13. P220: A de novo Xq13.2-13.3 duplication associated with non-syndromic intellectual disability
14. Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients
15. The contributions of oxytocin and vasopressin pathway genes to human behavior
16. Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy
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