1. Fang, Shuo-Gui, Xia, Tian-Liang, Fu, Jian-Chang, Zhong, Qian, Han, Fei. . BCL6-SPECC1L: A Novel Fusion Gene in Nasopharyngeal Carcinoma. In Technology in cancer research & treatment, 21, 15330338221139981. doi:10.1177/15330338221139981. https://pubmed.ncbi.nlm.nih.gov/36412101/
2. Bai, Shanshan, Geng, Yingnan, Duan, Huichuan, Yuan, Jie, Wei, Min. 2021. A novel p.Pro871Leu missense mutation in SPECC1L gene causing craniosynostosis in a patient. In Orthodontics & craniofacial research, 24, 480-485. doi:10.1111/ocr.12473. https://pubmed.ncbi.nlm.nih.gov/33527670/
3. Ma, Li, Zhang, Quan, Dong, Yujie, Li, Haoyang, Wang, Jinghui. 2020. SPECC1L-ALK: A novel gene fusion response to ALK inhibitors in non-small cell lung cancer. In Lung cancer (Amsterdam, Netherlands), 143, 97-100. doi:10.1016/j.lungcan.2020.03.017. https://pubmed.ncbi.nlm.nih.gov/32216970/
4. Migliore, Chiara, Vendramin, Anna, McKee, Shane, Licastro, Danilo, Meroni, Germana. 2022. SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome. In Genes, 13, . doi:10.3390/genes13020252. https://pubmed.ncbi.nlm.nih.gov/35205294/
5. Hall, Everett G, Wenger, Luke W, Wilson, Nathan R, Butali, Azeez, Saadi, Irfan. . SPECC1L regulates palate development downstream of IRF6. In Human molecular genetics, 29, 845-858. doi:10.1093/hmg/ddaa002. https://pubmed.ncbi.nlm.nih.gov/31943082/
6. Saadi, Irfan, Alkuraya, Fowzan S, Gisselbrecht, Stephen S, Erickson, Robert P, Maas, Richard L. 2011. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. In American journal of human genetics, 89, 44-55. doi:10.1016/j.ajhg.2011.05.023. https://pubmed.ncbi.nlm.nih.gov/21703590/
7. Wild, K Taylor, Gordon, Tia, Bhoj, Elizabeth J, Scott, Daryl A, Zackai, Elaine H. 2020. Congenital diaphragmatic hernia as a prominent feature of a SPECC1L-related syndrome. In American journal of medical genetics. Part A, 182, 2919-2925. doi:10.1002/ajmg.a.61878. https://pubmed.ncbi.nlm.nih.gov/32954677/
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