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(1 - 8 of 8)
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
Skewed X-inactivation is common in the general female population
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
Skewed X-inactivation is common in the general female population
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant
Susceptibility to Chronic Mucus Hypersecretion, a Genome Wide Association Study
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Multiple common variants for celiac disease influencing immune gene expression