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CHD3;jsessionid=8AAC087768642ABDDDB4719F787185A3;jsessionid=002B812A48FA6E90A66987BA73AAE563
(gene)
Summary
General Info
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Ciliary ganglion
Atrioventricular node
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Most Relevant Literature
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
A novel CHD3 variant in a patient with central precocious puberty: Expanded phenotype of Snijders Bl…
Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to …
A de novo CHD3 variant in a child with intellectual disability, autism, joint laxity, and dysmorphis…
Snijders Blok-Campeau syndrome caused by CHD3 gene mutation: a case report.
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There were no clinical trials for CHD3;jsessionid=8AAC087768642ABDDDB4719F787185A3;jsessionid=002B812A48FA6E90A66987BA73AAE563
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