1. Wang, Tao, Dou, Yi-Chen, Xuan, Zhao-Peng, Fu, Dong-Sheng, Lu, Lai-Jin. . Molecular Etiology in Thumb Polydactyly in Mutated GLI3 Mouse Gene. In Critical reviews in eukaryotic gene expression, 31, 69-83. doi:10.1615/CritRevEukaryotGeneExpr.2021038555. https://pubmed.ncbi.nlm.nih.gov/34936293/
2. Guo, Xiaoyan, Shi, Tengfei, Lin, Mingrui, Liu, Boling, Pan, Yuancheng. . Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families. In Genetic testing and molecular biomarkers, 27, 299-305. doi:10.1089/gtmb.2023.0022. https://pubmed.ncbi.nlm.nih.gov/37768332/
3. Letelier, Joaquín, Naranjo, Silvia, Sospedra-Arrufat, Ismael, Shubin, Neil, Gómez-Skarmeta, José Luis. . The Shh/Gli3 gene regulatory network precedes the origin of paired fins and reveals the deep homology between distal fins and digits. In Proceedings of the National Academy of Sciences of the United States of America, 118, . doi:10.1073/pnas.2100575118. https://pubmed.ncbi.nlm.nih.gov/34750251/
4. Matissek, Stephan J, Elsawa, Sherine F. 2020. GLI3: a mediator of genetic diseases, development and cancer. In Cell communication and signaling : CCS, 18, 54. doi:10.1186/s12964-020-00540-x. https://pubmed.ncbi.nlm.nih.gov/32245491/
5. McClelland, Kathryn, Li, Weili, Rosenblum, Norman D. 2022. Pallister-Hall syndrome, GLI3, and kidney malformation. In American journal of medical genetics. Part C, Seminars in medical genetics, 190, 264-278. doi:10.1002/ajmg.c.31999. https://pubmed.ncbi.nlm.nih.gov/36165461/
6. Naruse, Ichiro, Ueta, Etsuko, Sumino, Yoshiki, Ogawa, Masaya, Ishikiriyama, Satoshi. . Birth defects caused by mutations in human GLI3 and mouse Gli3 genes. In Congenital anomalies, 50, 1-7. doi:10.1111/j.1741-4520.2009.00266.x. https://pubmed.ncbi.nlm.nih.gov/20201963/
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