The Role of GPR56 in Neurofibromatosis type 1 Secondary to Scoliosis
Siyi Cai(Peking Union Medical College Hospital), Guixing Qiu(Peking Union Medical College Hospital)
Cited by 0
Related Papers
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
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome
|BMC Musculoskeletal Disorders|2020|32
Comparative proteomics analysis for identifying the lipid metabolism related pathways in patients with Klippel-Feil syndrome
|Annals of Translational Medicine|2021|3
Phenotype expansion of variants affecting p38 MAPK signaling in hypospadias patients
|Orphanet Journal of Rare Diseases|2022|3
The mutational burden and oligogenic inheritance in Klippel-Feil Syndrome
|Research Square|2020|0