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Journal of Inherited Metabolic Disease|January 1, 1993
Biochemical and immunological characterization of X-linked ichthyosisX Fan, L Petruschka, K Wulff, et al.
Haemostasis|September 1, 1996
Large-scale screening for factor V Leiden mutation in a north-eastern German populationW Schröder, M Koesling, K Wulff, et al.
Human Mutation|January 1, 1994
Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)W Schröder, K Wulff, M Wehnert, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDRF H Herrmann, T Kruse, M Wehnert, et al.
Neurobiology of Learning and Memory|July 14, 2020
Sleep-related memory consolidation in the psychosis spectrum phenotypeR J Purple, J Cosgrave, V Vyazovskiy, et al.
Clinical Genetics|January 1, 1994
Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regionsA M Gerdes, M B Petersen, H D Schrøder, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 21, 2011
Factor X deficiency and intracranial bleeding: who is at risk?R Rauch, M Girisch, G Wiegand, et al.
Pediatric Hematology and Oncology|May 3, 2006
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->AU Hennewig, S Eisert, K Wulff, et al.
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