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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.Journal of the American Veterinary Medical Association|August 1, 1992
Comparison of applanation tonometers in dogs and horsesJ Dziezyc, N J Millichamp, W B SmithOrganic Letters|September 28, 2001
Strongly UV absorbing bifunctional azoalkanesP S Engel, H Wu, W B SmithThe Journal of Allergy and Clinical Immunology|February 1, 1987
Spontaneous suppressor cell activity in patients with the acquired immune deficiency syndrome and associated conditionsH P Katner, R D deShazo, G A Pankey, et al.Pageof 18