LAUSR

Whole exome association of rare deletions in multiplex oral cleft families

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0 Published in 2017 at "Genetic Epidemiology"

DOI: 10.1002/gepi.22010

Abstract: By sequencing the exomes of distantly related individuals in multiplex families, rare mutational and structural changes to coding DNA can be characterized and their relationship to disease risk can be assessed. Recently, several rare single… read more here.

Keywords: risk; rare deletions; whole exome; families whole ... See more keywords