1. Arrabal, Luisa, Muñoz-Pujol, Gerard, Medina Martínez, Inmaculada, Tort, Frederic, Ribes, Antonia. 2023. Functional Evidence of CCDC186 as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations. In International journal of molecular sciences, 24, . doi:10.3390/ijms241512319. https://pubmed.ncbi.nlm.nih.gov/37569695/
2. Monies, Dorota, Abouelhoda, Mohamed, AlSayed, Moeenaldeen, Meyer, Brian F, Alkuraya, Fowzan S. 2017. The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes. In Human genetics, 136, 921-939. doi:10.1007/s00439-017-1821-8. https://pubmed.ncbi.nlm.nih.gov/28600779/
3. Brugger, Melanie, Becker-Dettling, Fiona, Brunet, Theresa, Borggraefe, Ingo, Wagner, Matias. 2020. A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy. In Annals of clinical and translational neurology, 8, 278-283. doi:10.1002/acn3.51260. https://pubmed.ncbi.nlm.nih.gov/33259146/
4. Liu, Y Y, Wu, S F, Liu, X D, Lu, L P, Zeng, X. . [Characteristics of RET gene rearrangement detected by fluorescence in situ hybridization in lung cancer]. In Zhonghua bing li xue za zhi = Chinese journal of pathology, 54, 36-40. doi:10.3760/cma.j.cn112151-20240722-00469. https://pubmed.ncbi.nlm.nih.gov/39762169/
5. Liu, Yuanyuan, Wu, Shafei, Zhou, Liangrui, Guo, Yong, Zeng, Xuan. . Pitfalls in RET Fusion Detection Using Break-Apart FISH Probes in Papillary Thyroid Carcinoma. In The Journal of clinical endocrinology and metabolism, 106, 1129-1138. doi:10.1210/clinem/dgaa913. https://pubmed.ncbi.nlm.nih.gov/33382428/
6. Rolfe, S M, Mao, D, Maga, A M. 2024. Streamlining Asymmetry Quantification in Fetal Mouse Imaging: A Semi-Automated Pipeline Supported by Expert Guidance. In bioRxiv : the preprint server for biology, , . doi:10.1101/2024.10.31.621187. https://pubmed.ncbi.nlm.nih.gov/39554050/
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