1. van der Spek, Jet, den Hoed, Joery, Snijders Blok, Lot, Fisher, Simon E, Kleefstra, Tjitske. 2022. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome. In Genetics in medicine : official journal of the American College of Medical Genetics, 24, 1283-1296. doi:10.1016/j.gim.2022.02.014. https://pubmed.ncbi.nlm.nih.gov/35346573/
2. Pascual, Patricia, Tenorio-Castano, Jair, Mignot, Cyril, Nevado, Julián, Lapunzina, Pablo. 2023. Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review. In Genes, 14, . doi:10.3390/genes14091664. https://pubmed.ncbi.nlm.nih.gov/37761804/
3. Chang, Soojeong, Yim, Sujin, Park, Hyunsung. 2019. The cancer driver genes IDH1/2, JARID1C/ KDM5C, and UTX/ KDM6A: crosstalk between histone demethylation and hypoxic reprogramming in cancer metabolism. In Experimental & molecular medicine, 51, 1-17. doi:10.1038/s12276-019-0230-6. https://pubmed.ncbi.nlm.nih.gov/31221981/
4. Fan, Xi-Yong. . Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report. In Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 23, 965-968. doi:10.7499/j.issn.1008-8830.2106091. https://pubmed.ncbi.nlm.nih.gov/34535214/
5. Pastorcic, Martine, Das, Hriday K. . The C-terminal region of CHD3/ZFH interacts with the CIDD region of the Ets transcription factor ERM and represses transcription of the human presenilin 1 gene. In The FEBS journal, 274, 1434-48. doi:. https://pubmed.ncbi.nlm.nih.gov/17489097/
6. Date, Yuki, Kondo, Hisatomo, Yamashita, Atsuko, Kasugai, Shohei, Ota, Masato S. 2020. Combined in silico analysis identified a putative tooth root formation-related gene, Chd3, which regulates DNA synthesis in HERS01a cells. In Odontology, 108, 386-395. doi:10.1007/s10266-020-00489-w. https://pubmed.ncbi.nlm.nih.gov/32026140/
7. Gao, Yuanyuan, Wang, Pei, Chen, Mengying, Zhang, Hongmei, Zhu, Min. 2024. Novel genotypes and phenotypes in Snijders Blok-Campeau syndrome caused by CHD3 mutations. In Frontiers in genetics, 15, 1347933. doi:10.3389/fgene.2024.1347933. https://pubmed.ncbi.nlm.nih.gov/39050258/
智鼠故事 
