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UnknownDVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome.
Not available
S-EPMC4385180 | biostudies-literature
UnknownWNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
Not available
S-EPMC5777383 | biostudies-literature
UnknownNovel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability.
Not available
S-EPMC8756549 | biostudies-literature
UnknownNovel risk loci for COVID-19 hospitalization among admixed American populations.
Not available
S-EPMC11449485 | biostudies-literature
UnknownNovel genes and sex differences in COVID-19 severity.
Not available
S-EPMC9652109 | biostudies-literature
UnknownGenetic patterns related to von Willebrand factor: implications on the need for mechanical ventilation, severity, and death in COVID-19.
Not available
S-EPMC12828584 | biostudies-literature
UnknownShaping current European mitochondrial haplogroup frequency in response to infection: the case of SARS-CoV-2 severity.
Not available
S-EPMC11718132 | biostudies-literature
UnknownClonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2.
Not available
S-EPMC10876565 | biostudies-literature
UnknownGWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19.
Not available
S-EPMC10208981 | biostudies-literature
UnknownA second update on mapping the human genetic architecture of COVID-19.
Not available
S-EPMC10482689 | biostudies-literature
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