Genetic research progress in congenital craniosynostosis
Article in Chinese Journal of Plastic Surgery (May 2022)
The most recent citing publications are shown below. View all 18 publications that cite this research output on Dimensions.
Comprehensive functional network analysis and screening of deleterious pathogenic variants in non-syndromic hearing loss causative genes
Article in Bioscience Reports (October 2021)
Autopsy Case of Pfeiffer Syndrome Type 2, a Phenotype of Fibroblast Growth Factor Receptor-Associated Craniosynostosis Syndromes, with Tracheal Cartilage Sleeve and Abnormal Hyperplasia of Bronchial Cartilages
Article in American Journal of Case Reports (June 2021)