ENA0000GenomicsMultiomicsUKSHhttps://www.ebi.ac.uk/ena/browser/view/PRJNA208271Homo sapiensIn a subset of imprinting disorders caused by epimutations, multiple imprinted loci are affected. We have investigated the clinical and molecular features of a familial DNA methylation disorder. Overall design: Bisulphite converted DNA from the 60 samples were hybridised to the Illumina Infinium 27k Human Methylation BeadchipENAmolecular disease, hereditary diseases, thymus nucleic acid, Methylations., DNS, (Deoxyribonucleotide)n, inherited genetic disease, hereditary disease or disorder, DNAn+1, inborn disorder, Double Stranded, genetic disorder, Deoxyribonucleic acid, Double-Stranded, genetic disease, familial disorder, Deoxyribonucleic acids, (Deoxyribonucleotide)n+m, hereditary disease, genetic condition, Deoxyribonucleic Acid, ds DNA, Desoxyribonukleinsaeure, Double-Stranded DNA, (Deoxyribonucleotide)m, DNA, deoxyribonucleic acids, methylation, DNAn, ds-DNA, inherited disease, desoxyribose nucleic acid, Mendelian diseasehuman being, human., man0.00.00.00.00.00falseHomo sapiensA familial disorder of altered DNA-methylation2022-05-122014-07-03PRJNA208271GSE47879241308169606