1. Huang, Lei, Yuan, Xiaodong, Zhao, Liangchao, Wang, Junqing, Shi, Yan. . Gene signature developed for predicting early relapse and survival in early-stage pancreatic cancer. In BJS open, 7, . doi:10.1093/bjsopen/zrad031. https://pubmed.ncbi.nlm.nih.gov/37196196/
2. Park, Elizabeth M, Scott, Phillip M, Clutario, Kevin, Gerber, Scott A, Holland, Andrew J. 2019. WBP11 is required for splicing the TUBGCP6 pre-mRNA to promote centriole duplication. In The Journal of cell biology, 219, . doi:10.1083/jcb.201904203. https://pubmed.ncbi.nlm.nih.gov/31874114/
3. Xie, Han, Ma, Jiayi, Ji, Taoyun, Cai, Lixin, Wu, Ye. 2022. Vagus nerve stimulation in children with drug-resistant epilepsy of monogenic etiology. In Frontiers in neurology, 13, 951850. doi:10.3389/fneur.2022.951850. https://pubmed.ncbi.nlm.nih.gov/36119689/
4. Chen, Feifei, Lei, Tingying, Fu, Fang, Pan, Min, Liao, Can. . [Application of chromosome microarray analysis for fetuses with multicystic dysplastic kidney]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 33, 752-757. doi:. https://pubmed.ncbi.nlm.nih.gov/27984599/
5. Hasan, Mohammed Nihal, Razvi, Syed Shoeb, Choudhry, Hani, Asami, Tadao, Alhosin, Mahmoud. 2019. Gene Ontology and Expression Studies of Strigolactone Analogues on a Hepatocellular Carcinoma Cell Line. In Analytical cellular pathology (Amsterdam), 2019, 1598182. doi:10.1155/2019/1598182. https://pubmed.ncbi.nlm.nih.gov/31482051/
6. Maver, Aleš, Čuturilo, Goran, Kovanda, Anja, Miletić, Aleksandra, Peterlin, Borut. 2018. Rare missense TUBGCP5 gene variant in a patient with primary microcephaly. In European journal of medical genetics, 62, 103598. doi:10.1016/j.ejmg.2018.12.003. https://pubmed.ncbi.nlm.nih.gov/30543990/
7. Kolbjer, Sintia, Martin, Daniel A, Pettersson, Maria, Dahlin, Maria, Anderlid, Britt-Marie. 2021. Lissencephaly in an epilepsy cohort: Molecular, radiological and clinical aspects. In European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 30, 71-81. doi:10.1016/j.ejpn.2020.12.011. https://pubmed.ncbi.nlm.nih.gov/33453472/
8. Hull, Sarah, Arno, Gavin, Ostergaard, Pia, Moore, Anthony T, Michaelides, Michel. 2019. Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly. In American journal of ophthalmology, 207, 87-98. doi:10.1016/j.ajo.2019.05.001. https://pubmed.ncbi.nlm.nih.gov/31077665/
智鼠故事 
