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2020
(2)
2022
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The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.
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S-EPMC7719554
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biostudies-literature
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Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.
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S-EPMC9069069
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biostudies-literature
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Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7.
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S-EPMC8093014
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biostudies-literature
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