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UnknownTransgenerational impact of intimate partner violence on methylation in the promoter of the glucocorticoid receptor.
Not available
S-EPMC3309516 | biostudies-literature
UnknownFunctional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive.
Not available
S-EPMC12807467 | biostudies-literature
UnknownA Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
Not available
S-EPMC6174323 | biostudies-literature
UnknownDe Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder.
Not available
S-EPMC5992133 | biostudies-literature
UnknownTelomere length is not a main factor for the development of islet autoimmunity and type 1 diabetes in the TEDDY study.
Not available
S-EPMC8927592 | biostudies-literature
UnknownGenome Sequencing for Diagnosing Rare Diseases.
Not available
S-EPMC11350637 | biostudies-literature
UnknownBeyond species means - the intraspecific contribution to global wood density variation.
Not available
S-EPMC12917463 | biostudies-literature
UnknownGenetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Not available
S-EPMC5798660 | biostudies-literature
UnknownGenetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
Not available
S-EPMC4189926 | biostudies-literature
UnknownGenome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Not available
S-EPMC6288131 | biostudies-literature
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