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Paper Details

Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion.
Clin Epigenetics
15
2018
1, 17q12 deletion, 17q12 deletion locus, 17q12 microdeletion, DMPs, HNF1B, HNF1B genotype, HNF1B intragenic, Illumina 450K DNA methylation array, chromosome 17q12, deleted region, diabetes, differentially methylated probes, haploinsufficiency, monogenetic developmental renal disease, neurodevelopmental disorders, patient, patients, probes, transcription factor HNF1B
Author NameAffiliation
Joe BurrageUniversity of Exeter Medical School, University of Exeter
Eilis HannonUniversity of Exeter Medical School, University of Exeter
Jonathan MillUniversity of Exeter Medical School, University of Exeter
Jonathan MillUniversity of Exeter Medical School, University of Exeter
Andrew T HattersleyUniversity of Exeter Medical School, University of Exeter
Emma L DempsterUniversity of Exeter Medical School, University of Exeter
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Release 1.2