학술논문

Identification of rare de novo epigenetic variations in congenital disorders.
Document Type
Article
Source
Nature Communications; 5/25/2018, Vol. 9 Issue 1, p1-11, 11p
Subject
EPIGENETICS
CONGENITAL disorders
NUCLEOTIDE sequencing
DNA methylation
GENETIC mutation
Language
ISSN
20411723
Abstract
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