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Human Mutation, ISSN 1059-7794, 02/2012, Volume 33, Issue 2, pp. 343 - 350
Journal Article
Human Mutation, ISSN 1059-7794, 09/2018, Volume 39, Issue 9, pp. 1226 - 1237
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 06/2016, Volume 24, Issue 6, pp. 784 - 793
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 02/2018, Volume 36, Issue 4_suppl, pp. 718 - 718
Journal Article
Genetics and Molecular Biology, ISSN 1415-4757, 2012, Volume 35, Issue 4, pp. 714 - 724
The most frequent epigenetic alterations in Wilms tumor (WT) occur at WT2, assigned to 11p15. WT2 consists of two domains: telomeric domain 1 (DMRH19) that... 
Histopathology | Epigenetic | Methylation | MS-MLPA | Pyrosequencing | H19 LOCUS | epigenetic | BIOCHEMISTRY & MOLECULAR BIOLOGY | IMPRINTING DEFECTS | histopathology | pyrosequencing | 11P15 ABNORMALITIES | EPIGENETIC CHANGES | BECKWITH-WIEDEMANN-SYNDROME | IGF2/H19 LOCUS | methylation | DNA | GENETICS & HEREDITY | BWS | Human and Medical Genetics
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2016, Volume 170, Issue 10, pp. 2740 - 2749
Journal Article
Journal Article
Epigenomics, ISSN 1750-1911, 07/2018, Volume 10, Issue 7, pp. 941 - 954
Aim: This study aimed to establish a catalog of probes corresponding to imprinted differentially methylated regions (DMRs) on the Infinium HumanMethylationEPIC... 
imprinting | DNA methylation | uniparental diploidy | HUMAN GENOME | REGIONS | GENES | GENETICS & HEREDITY | UNIPARENTAL DISOMY | IMPRINTING DISORDERS | HYPOMETHYLATION
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2017, Volume 173, Issue 3, pp. 601 - 610
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 01/2013, Volume 161, Issue 1, pp. 192 - 197
Journal Article