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S41467-018-06014-6
S41467-018-06014-6
http://dx.doi.org/10.1038/S41467-018-06014-6
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
P356
Q58611455-FCB01E59-94DE-4557-9C19-E69B3A10D226
P356
S41467-018-06014-6
http://dx.doi.org/10.1038/S41467-018-06014-6