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B.S. Andresen (B.), S. Olpin (S.), E.A. Kvittingen (E.), P. Augoustides-Savvopoulou (Persa), D. Lindhout (Dick), D.J.J. Halley (Dicky), C. Vianey-Saban (C.), R.J.A. Wanders (Ronald), L. Ijlst (L.), L.D. Schroeder (L.), et al. L. Bolund (L.) and P.K. Gregersen (Peter )

1999-06-15

DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency

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Journal of Inherited Metabolic Disease , Volume 22 - Issue 3 p. 281- 285

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Persistent URL doi.org/10.1023/A:1005558828223, hdl.handle.net/1765/52242
Journal Journal of Inherited Metabolic Disease
Organisation Department of Clinical Genetics
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Andresen, B., Olpin, S., Kvittingen, E., Augoustides-Savvopoulou, P., Lindhout, D., Halley, D., … Gregersen, P. (1999). DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency. In Journal of Inherited Metabolic Disease (Vol. 22, pp. 281–285). doi:10.1023/A:1005558828223
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