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Characterizing Long COVID Symptoms During Early Childhood.
Not available
S-EPMC12117493
|
biostudies-literature
Cite
The impact of low-mode symmetry on inertial fusion energy output in the burning plasma state.
Not available
S-EPMC10998902
|
biostudies-literature
Cite
Macrocephaly and developmental delay caused by missense variants in RAB5C.
Not available
S-EPMC10586195
|
biostudies-literature
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Elliptic anisotropy measurement of the f<sub>0</sub>(980) hadron in proton-lead collisions and evidence for its quark-antiquark composition.
Not available
S-EPMC12391314
|
biostudies-literature
Cite
Tocilizumab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC8084355
|
biostudies-literature
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Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples.
Not available
S-EPMC8664895
|
biostudies-literature
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Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation.
Not available
S-EPMC11305122
|
biostudies-literature
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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
Gain-of-function mutations in <i>ALPK1</i> cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Not available
S-EPMC9484401
|
biostudies-literature
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Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder.
Not available
S-EPMC11451386
|
biostudies-literature
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