Sort   by:  
 Page size 
UnknownDysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy.
Not available
S-EPMC4817901 | biostudies-literature
UnknownDescribing the genetic architecture of epilepsy through heritability analysis.
Not available
S-EPMC4163034 | biostudies-literature
UnknownA genetic study of Wilson's disease in the United Kingdom.
Not available
S-EPMC3634195 | biostudies-literature
UnknownObstructive sleep apnoea and the risk for coronary heart disease and type 2 diabetes: a longitudinal population-based study in Finland.
Not available
S-EPMC6194468 | biostudies-literature
UnknownAssociation of the timing of puberty with a chromosome 2 locus.
Not available
S-EPMC2685475 | biostudies-literature
UnknownGenetic risk prediction and a 2-stage risk screening strategy for coronary heart disease.
Not available
S-EPMC4210840 | biostudies-literature
UnknownDiagnosing migraine from genome-wide genotype data: a machine learning analysis.
Not available
S-EPMC12782171 | biostudies-literature
UnknownSerum calcium and risk of migraine: a Mendelian randomization study.
Not available
S-EPMC5409060 | biostudies-literature
UnknownAssignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.
Not available
S-EPMC1377549 | biostudies-literature
UnknownTowards a European consensus for reporting incidental findings during clinical NGS testing.
Not available
S-EPMC4795187 | biostudies-literature
Sort   by:  
 Page size