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ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants
Free accessOnline Contents | 2021| -
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
Free accessBASE | 2020| -
The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision
Free accessBASE | 2022| -
Proceedings of the 13th International Newborn Brain Conference: Neonatal Neurocritical Care, Seizures, and Continuous EEG monitoring
Free accessVirtual conference, February 10th-12th 2022IOS Press | 2022|
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