ELIZABETH ROEDER to Whole Genome Sequencing
This is a "connection" page, showing publications ELIZABETH ROEDER has written about Whole Genome Sequencing.
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Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype. Hum Mutat. 2017 12; 38(12):1774-1785.
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Identification of novel candidate disease genes from de novo exonic copy number variants. Genome Med. 2017 09 21; 9(1):83.
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