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. 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/
4. Tanaka, Mikiko. 2016. Fins into limbs: Autopod acquisition and anterior elements reduction by modifying gene networks involving 5'Hox, Gli3, and Shh. In Developmental biology, 413, 1-7. doi:10.1016/j.ydbio.2016.03.007. https://pubmed.ncbi.nlm.nih.gov/26992366/
5. 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/
6. Hou, Xinwei, Wang, Jianjun, Lu, Yi, Yang, Huirong, Wu, Kai. . [Analysis of variant of GLI3 gene in a child featuring autosomal dominant Pallister-Hall syndrome]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 40, 92-95. doi:10.3760/cma.j.cn511374-20220224-00125. https://pubmed.ncbi.nlm.nih.gov/36585009/
7. 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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