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K Wulff

Showing results (81-90 of 118) with videos related to

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Lancet (London, England)|January 6, 1996
World distribution of factor V Leiden mutationW Schröder, M Koessling, 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.
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.
American Journal of Medical Genetics|June 19, 1995
Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish countyM B Petersen, K Brøndum-Nielsen, L K Hansen, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Genetic diagnosis in classical phenylketonuria]K Wulff, F H Herrmann, 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.
Human Mutation|February 19, 2000
Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 geneK Wulff, H Gazda, W Schröder, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
Lancet (London, England)|January 6, 1996
World distribution of factor V Leiden mutationW Schröder, M Koessling, 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.
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.
American Journal of Medical Genetics|June 19, 1995
Clinical, cytogenetic, and molecular diagnosis of Angelman syndrome: estimated prevalence rate in a Danish countyM B Petersen, K Brøndum-Nielsen, L K Hansen, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Genetic diagnosis in classical phenylketonuria]K Wulff, F H Herrmann, 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.
Human Mutation|February 19, 2000
Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 geneK Wulff, H Gazda, W Schröder, et al.
Pageof 12