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2023
(2)
2021
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Dominant negative variants in
IKZF2
cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.
Not available
S-EPMC11206234
|
biostudies-literature
Cite
A second update on mapping the human genetic architecture of COVID-19.
Not available
S-EPMC10482689
|
biostudies-literature
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Clinical Outcomes and Response to Vericiguat According to Index Heart Failure Event: Insights From the VICTORIA Trial.
Not available
S-EPMC7666431
|
biostudies-literature
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OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
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