doi.org/10.1023/A:1005558828223, hdl.handle.net/1765/52242
Journal of Inherited Metabolic Disease
Department of Clinical Genetics

Andresen, B., Olpin, S., Kvittingen, E., Augoustides-Savvopoulou, P., Lindhout, D., Halley, D., Vianey-Saban, C., Wanders, R., Ijlst, L., Schroeder, L., Bolund, L.& Gregersen, P. (1999). DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease, 22(3), 281–285.https://doi.org/10.1023/A:1005558828223