QuickView for CHD3;jsessionid=8AAC087768642ABDDDB4719F787185A3;jsessionid=002B812A48FA6E90A66987BA73AAE563;jsessionid=1B2727472ED38166B921BC52956020D6;jsessionid=615951F3539BCC1EC1FC695660754CF5;jsessionid=966984F83B521CEBAB88BA8B0BFF94A4;jsessionid=A6E14581923F8707D30303476F22BF86 (gene)

1. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
2. A novel CHD3 variant in a patient with central precocious puberty: Expanded phenotype of Snijders Bl…
3. Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to …
4. A de novo CHD3 variant in a child with intellectual disability, autism, joint laxity, and dysmorphis…
5. Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report.

There were no clinical trials for CHD3;jsessionid=8AAC087768642ABDDDB4719F787185A3;jsessionid=002B812A48FA6E90A66987BA73AAE563;jsessionid=1B2727472ED38166B921BC52956020D6;jsessionid=615951F3539BCC1EC1FC695660754CF5;jsessionid=966984F83B521CEBAB88BA8B0BFF94A4;jsessionid=A6E14581923F8707D30303476F22BF86