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2025
(1)
2021
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Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Not available
S-EPMC8278787
|
biostudies-literature
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Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes.
Not available
S-EPMC12551315
|
biostudies-literature
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OmicsDI
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OmicsDI is an Elixir interoperability service.
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