A novel Xp22.13 microdeletion in Nance-Horan syndrome.
Andrea AccogliMonica TraversoFrancesca MadiaTommaso BelliniMaria Stella VariFrancesca PintoValeria CapraPublished in: Birth defects research (2017)
We compare our case with the previous Xp22.13 microdeletions and discuss the possible pathogenetic role of the flanking genes. Birth Defects Research 109:866-868, 2017. © 2017 Wiley Periodicals, Inc.