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. Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Fisher, Simon E, Campeau, Philippe M. 2018. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. In Nature communications, 9, 4619. doi:10.1038/s41467-018-06014-6. https://pubmed.ncbi.nlm.nih.gov/30397230/
4. 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/
5. 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/
6. Rodríguez-Castañeda, Fernando, Lemma, Roza Berhanu, Cuervo, Ignacio, Eskeland, Ragnhild, Gabrielsen, Odd Stokke. 2018. The SUMO protease SENP1 and the chromatin remodeler CHD3 interact and jointly affect chromatin accessibility and gene expression. In The Journal of biological chemistry, 293, 15439-15454. doi:10.1074/jbc.RA118.002844. https://pubmed.ncbi.nlm.nih.gov/30082317/
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