Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis
Lianlei Wang(Qilu Hospital of Shandong University), Nan Wu(Chongqing University)
Cited by 1
Related Papers
<i>TBX6</i> Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
|New England Journal of Medicine|2015|317
Reanalysis of Clinical Exome Sequencing Data
|New England Journal of Medicine|2019|303
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
|Genetics in Medicine|2019|94
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
|The American Journal of Human Genetics|2021|90