G Seidlitz

First prenatal diagnosis of acyl‐CoA oxidase deficiency

Ronald J. A. Wanders, A. Schelen, N Feller et al. · Journal of Inherited Metabolic Disease · 1990 · 41 citations

Medicine, Biochemistry, Obstetrics +13

Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene

Marie‐Louise Steén‐Bondeson, Niklas Dahl, T. Tønnesen et al. · Human Molecular Genetics · 1992 · 31 citations

Life Sciences, Genetics, Molecular Genetics +15

Mutations of the iduronate-2-sulfatase (IDS) gene in patients with hunter syndrome (mucopolysaccharidosis II)

W. Schröder, K. Wulff, Manfred Wehnert et al. · Human Mutation · 1994 · 23 citations

Life Sciences, Genetics, Molecular Genetics +17

Hereditary Orotic Aciduria with Epilepsy and without Megaloblastic Anemia

Heinz Lauffer, Peter Lauenstein, Georg Hoffmann et al. · Neuropediatrics · 2015 · 22 citations

Medicine, Hematology, Neurology +13

German Maternal Phenylketonuria Study

Sanja Cipcic-Schmidt, Friedrich K. Trefz, B. Fünders et al. · European Journal of Pediatrics · 1996 · 18 citations

Medicine, Maternal Health, Obstetrics +3