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Paper Details

Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities.
Eur J Hum Genet
46
2017
DNA, KMT2A, KMT2D, Kabuki syndrome, Patients, Wiedermann-Steiner syndrome, abnormalities of DNA methylation, histone, inborn errors of, monogenic disorder, patients
Author NameAffiliation
Nara SobreiraMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Nara SobreiraJohns Hopkins University School of Medicine
Christine Ladd-AcostaJohns Hopkins Bloomberg School of Public Health
Kimberly F DohenyCenter for Inherited Disease Research (CIDR), Institute of Genetic Medicine, Johns Hopkins University School of Medicine
David ValleMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
David ValleJohns Hopkins University School of Medicine
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