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UnknownDistinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype.
Not available
S-EPMC6731376 | biostudies-literature
UnknownMulti-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.
Not available
S-EPMC10165422 | biostudies-literature
UnknownA Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.
Not available
S-EPMC5712232 | biostudies-literature
UnknownNovel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome.
Not available
S-EPMC11068106 | biostudies-literature
UnknownA programmed decline in ribosome levels governs human early neurodevelopment.
Not available
S-EPMC12339376 | biostudies-literature
UnknownEffect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease: A Randomized Clinical Trial.
Not available
S-EPMC8058640 | biostudies-literature
UnknownRole of the repeat expansion size in predicting age of onset and severity in RFC1 disease.
Not available
S-EPMC11068103 | biostudies-literature
UnknownSynthetic ZFTA fusions pinpoint disordered protein domain acquisition as a mechanism of brain tumorigenesis.
Not available
S-EPMC12431856 | biostudies-literature
UnknownMLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.
Not available
S-EPMC4686660 | biostudies-literature
UnknownNCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism.
Not available
S-EPMC7674997 | biostudies-literature
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