Prenatal diagnosis of congenital disorder of glycosylation type Ia (CDG-Ia) by cordocentesis and transferrin isoelectric focussing of serum of a 27-week fetus with non-immune hydrops

Matthew Edwards, Fiona McKenzie, Stephen O'Callaghan, David Somerset, Phillip Woodford, Jillian Spilsbury, Michael Fietz, Janice Fletcher

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