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3. Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

4. Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis

5. RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

6. Impaired glycine neurotransmission causes adolescent idiopathic scoliosis

8. Association of an estrogen-sensitive Pax1-Col11a1-Mmp3 signaling axis with adolescent idiopathic scoliosis

9. Association of an estrogen-sensitive Pax1-Col11a1-Mmp3 signaling axis with adolescent idiopathic scoliosis

10. Do Children With Medicaid Insurance Have Increased Revision Rates 5 Years After Posterior Spinal Fusions?

21. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome

22. Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study

23. Association of an estrogen-sensitive Pax1-Col11a1-Mmp3 signaling axis with adolescent idiopathic scoliosis

33. Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

36. Thousands of induced germline mutations affecting immune cells identified by automated meiotic mapping coupled with machine learning

37. Saturation mutagenesis defines novel mouse models of severe spine deformity

38. Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice

44. Genetic association and characterization ofFSTL5in isolated clubfoot

46. Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci

48. Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

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