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Sahai, Inderneel

One or more keywords matched the following items that are connected to Sahai, Inderneel

Item Type	Name
Academic Article	CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Academic Article	Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.
Concept	Neurodevelopmental Disorders
Academic Article	Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases.

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