Additional file 2: of Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

Clissold, Rhian; Ashfield, Beth; Burrage, Joe; Hannon, Eilis; Bingham, Coralie; Mill, Jonathan; Hattersley, Andrew; Dempster, Emma

doi:10.6084/m9.figshare.6838691.v1

13148_2018_530_MOESM2_ESM.pdf (15.15 kB)

Additional file 2: of Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

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posted on 2018-07-18, 05:00 authored by Rhian Clissold, Beth Ashfield, Joe Burrage, Eilis Hannon, Coralie Bingham, Jonathan Mill, Andrew Hattersley, Emma Dempster

Figure S1. This figure illustrates the extent of the 17q12 deletion in each patient as estimated by the CNV calling algorithm within the CHAMP package. (PDF 15 kb)

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Medical Research Council

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Epigenetics DNA methylation HNF1B CNV 17q12 deletion Renal disease Autism

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Additional file 2: of Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

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