38 results on '"Wang, Xike"'
Search Results
2. The intervention dilemma and high burden of children with autism in Guizhou province, Southwest China
3. Mapping Multi-view Architecture Products to Multi-agent Software Architecture Style
4. Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population
5. Magnetic properties of FePc sheet modified by the adsorption of gas molecules
6. Magnetic Properties of the Gas Molecules Adsorbed on the Fepc Sheet
7. Rh-CXCL-12 Attenuates Neuronal Pyroptosis after Subarachnoid Hemorrhage in Rats via Regulating the CXCR4/NLRP1 Pathway
8. A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review
9. Homozygosity for a novel missense variant of RPGRIP1L causing Joubert syndrome with renal defects in a family of Chinese descent
10. Mapping Multi-view Architecture Products to Multi-agent Software Architecture Style
11. Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree
12. Corrigendum to: A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage
13. A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage
14. Identification of two CUL7 variants in two Chinese families with 3‐M syndrome by whole‐exome sequencing
15. Novel joint catalytic properties of Fe and N co-doped graphene for CO oxidation
16. Internal friction peak and damping mechanism in high damping 6061Al/SiC p/Gr hybrid metal matrix composite
17. Novel TRAPPC11 Mutations in a Chinese Pedigree of Limb Girdle Muscular Dystrophy
18. Ambient Air Pollution and Daily Hospital Admissions for Respiratory Disease in Children in Guiyang, China
19. Thymidylate synthase gene variation is associated with the risk for conotruncal heart defects in Chinese population
20. Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice
21. gene variation is associated with the risk for conotruncal heart defects in Chinese population.
22. Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice.
23. Thymidylate synthasegene variation is associated with the risk for conotruncal heart defects in Chinese population
24. A structure-oriented agent organization model based on multi-views architecture products of complicated information system
25. Identification of Two Novel Mutations in Patients With X-Linked Primary Immunodeficiencies
26. Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy
27. Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects
28. Influence of genes and the environment in familial congenital heart defects
29. A Potential Relationship among Beta-Defensins Haplotype, SOX7 Duplication and Cardiac Defects
30. Familial congenital heart disease: data collection and preliminary analysis
31. Mapping Multi-Views Architecture Products of Complicated Information System to Agent Organizations
32. Identification of Two Novel Mutations in Patients With X-Linked Primary Immunodeficiencies.
33. Internal friction peak and damping mechanism in high damping 6061Al/SiCp/Gr hybrid metal matrix composite
34. Familial congenital heart disease: data collection and preliminary analysis.
35. Internal friction peak and damping mechanism in high damping 6061Al/SiCp/Gr hybrid metal matrix composite
36. Thymidylate synthase gene variation is associated with the risk for conotruncal heart defects in Chinese population.
37. [Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect].
38. Influence of genes and the environment in familial congenital heart defects.
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