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UnknownAn ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Not available
S-EPMC8263055 | biostudies-literature
UnknownCentral corneal thickness in children.
Not available
S-EPMC3253021 | biostudies-literature
UnknownIntraobserver reliability of contact pachymetry in children.
Not available
S-EPMC3639436 | biostudies-literature
UnknownNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
Not available
S-EPMC3772747 | biostudies-literature
UnknownNew-onset atrial fibrillation and chronic coronary syndrome in the CLARIFY registry.
Not available
S-EPMC10834159 | biostudies-literature
UnknownBiallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913 | biostudies-literature
UnknownA second update on mapping the human genetic architecture of COVID-19.
Not available
S-EPMC10482689 | biostudies-literature
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