T. Munce

发表

Early diagnosis of adenylosuccinate lyase deficiency using a high‐throughput screening method and a trial of oral S‐adenosyl‐l‐methionine as a treatment method

J. Freeman, J. Pitt, J. Duley, 2013, Developmental medicine and child neurology.

Molecular characterization of Prader-Willi syndrome by real-time PCR.

F. Bowling, Robert Simpson, T. Munce, 2008, Genetic testing.

Analysis of N- and O-linked protein glycosylation in children with Prader-Willi syndrome.

H. Heussler, F. Bowling, T. Munce, 2010, Journal of intellectual disability research : JIDR.