スポンサーリンク
Laboratory of Bone and Joint Diseases, Center for Genomic Medicine | 論文
- SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese
- A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
- Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers
- A Replication Study for Association of 5 Single Nucleotide Polymorphisms With Curve Progression of Adolescent Idiopathic Scoliosis in Japanese Patients