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

Research output: Contribution to journal › Article › peer-review

31 Citations (Scopus)

Fingerprint

Dive into the research topics of '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'. Together they form a unique fingerprint.

Medicine & Life Sciences