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spinal curvatures; scoliosis; idiopathic; DNA methylation; pyrosequencing; estrogen receptor 1; ESR1; scoliosis progression; adolescent idiopathic scoliosis; idiopathic scoliosis; exome sequencing; spine; polygenic; variants; musculoskeletal disease; cytoskeleton; extracellular matrix; contracture; arthrogryposis; congenital; POC5; cilia; genetics; spine deformity; genetic predisposition; complex trait; model animal; genome wide association study; genetic linkage study; Amyoplasia; DECIPHER (DatabasE of genomiC variation and Phenotype in Humans using Ensemble Resources); CNV (copy number variant); DA (distal arthrogryposis); IPA (ingenuity pathway analysis); HPO (human phenotype ontology); akinesia; MYOD; IGF2; FGFR1 (Fibroblast growth factor receptor 1); genetic variations; congenital scoliosis; monozygotic twin; epigenome-wide association study; bone; discordant; curve severity; differentially methylated region; congenital vertebral malformation; copy number variant; CNV; CHRNG; distal arthrogryposis type 8; Escobar; multiple pterygium syndrome; MYH3; protein tyrosine kinase 7 (PTK7); whole exome sequencing; n/a