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3. Integrated Analysis of the Association Between Variants at PAX7 and NSCL/P in the Han Population.

5. Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees.

8. A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome.

9. A Novel Missense Variant in the TCOF1Gene in one Chinese Case With Treacher Collins Syndrome

10. Identified a novel splicing mutation at EDA gene in a hypohidrotic ectodermal dysplasia pedigree.

13. sj-docx-1-cpc-10.1177_10556656231163398 - Supplemental material for Integrated Analysis of the Association Between Variants at PAX7 and NSCL/P in the Han Population

14. sj-docx-1-cpc-10.1177_10556656231157575 - Supplemental material for Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees

20. sj-docx-1-cpc-10.1177_10556656221125387 - Supplemental material for A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome

22. Identification of putative regulatory single-nucleotide variants in NTN1gene associated with NSCL/P

24. Association Between SNPs in 1q32.2 and NSCL ±  P in Han Chinese Population.

25. Association analysis of SNPs in GRHL3, FAF1, and KCNJ2 with NSCPO sub‐phenotypes in Han Chinese.

27. sj-docx-1-cpc-10.1177_10556656211052837 - Supplemental material for Association Between SNPs in 1q32.2 and NSCL �� P in Han Chinese Population

29. Association Between SNPs in 1q32.2 and NSCL ± Pin Han Chinese Population

31. SNPs at TP63 gene was specifically associated with right‐side cleft lip in Han Chinese population.

32. Effect of modified compound calcium phosphate cement on the differentiation and osteogenesis of bone mesenchymal stem cells

35. NTN1 gene was risk to non‐syndromic cleft lip only among Han Chinese population.

36. Causal Variations at IRF6Gene Identified in Van der Woude Syndrome Pedigrees

37. Integrated Analysis of the Association Between Variants at PAX7and NSCL/P in the Han Population

42. Integrated Analysis of the Association Between Variants at PAX7 and NSCL/P in the Han Population.

43. Causal Variations at IRF6 Gene Identified in Van der Woude Syndrome Pedigrees.

44. Review on the Role of IRF6 in the Pathogenesis of Non-syndromic Orofacial Clefts.

45. A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome.

46. Association Between SNPs in 1q32.2 and NSCL ±  P in Han Chinese Population.

47. [Association between platelet-derived growth factor-C single nucleotide polymorphisms and nonsyndromic cleft lip with or without cleft palate in Western Chinese population].

48. [Environmental factors of non-syndromic cleft lip and palate].

49. Exon sequencing reveals that missense mutation of PBX1 gene may increase the risk of non-syndromic cleft lip/palate.

50. [Pathogenic genes and clinical therapeutic strategies for Treacher Collins syndrome].

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