QuickView for CHD3;jsessionid=960422609D2A9E4AEB1F43E0CCB14650 (gene)

1. A severe neurocognitive phenotype caused by biallelic CHD3 variants in two siblings.
2. Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and L…
3. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
4. A novel CHD3 variant in a patient with central precocious puberty: Expanded phenotype of Snijders Bl…
5. Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to …

There were no clinical trials for CHD3;jsessionid=960422609D2A9E4AEB1F43E0CCB14650