1. Huber, Céline, Munnich, Arnold, Cormier-Daire, Valerie. . The 3M syndrome. In Best practice & research. Clinical endocrinology & metabolism, 25, 143-51. doi:10.1016/j.beem.2010.08.015. https://pubmed.ncbi.nlm.nih.gov/21396581/
2. Huber, Celine, Fradin, Mélanie, Edouard, Thomas, Munnich, Arnold, Cormier-Daire, Valerie. . OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels. In Human mutation, 31, 20-6. doi:10.1002/humu.21150. https://pubmed.ncbi.nlm.nih.gov/19877176/
3. Luo, Ming-Ran, Dai, Si-Ming, Li, Yin, Zhao, Shu-Jie, Yin, Guo-Yong. . 3M syndrome patient with a novel mutation: A case report. In World journal of clinical cases, 12, 1454-1460. doi:10.12998/wjcc.v12.i8.1454. https://pubmed.ncbi.nlm.nih.gov/38576808/
4. Simsek-Kiper, Pelin Ozlem, Taskiran, Ekim, Kosukcu, Can, Alikasifoglu, Mehmet, Boduroglu, Koray. 2019. Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. In American journal of medical genetics. Part A, 179, 1157-1172. doi:10.1002/ajmg.a.61154. https://pubmed.ncbi.nlm.nih.gov/30980518/
智鼠故事 
