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F H Herrmann

Showing results (21-30 of 66) with videos related to

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Human Genetics|June 1, 1992
Structural gene aberrations in mucopolysaccharidosis II (Hunter)M Wehnert, J J Hopwood, W Schröder, et al.
Acta Dermato-Venereologica|January 1, 1990
Proliferation and differentiation of cultured epidermal cells from patients with X-linked ichthyosis and ichthyosis vulgarisP K Jensen, F H Herrmann, J Hadlich, et al.
Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Human Mutation|January 1, 1997
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophyK Wulff, J E Parrish, F H Herrmann, 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.
Acta Haematologica|January 1, 1982
The effect of diamide (azodicarboxylic acid-bis-dimethylamide) on sulfhydryl group content, proteins, and the location of phosphatidylethanolamine in human blood plateletsG Ostermann, P Spangenberg, M Meyer, 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.
Zentralblatt Fur Gynakologie|January 1, 1985
[45,X/46,X,del(Yq) sex chromosome mosaicism--analysis of the phenotypic expression]W Werner, B John, U Tuschy, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Pageof 7

Showing results (21-30 of 66) with videos related to

Sort By:
Pageof 7
Human Genetics|June 1, 1992
Structural gene aberrations in mucopolysaccharidosis II (Hunter)M Wehnert, J J Hopwood, W Schröder, et al.
Acta Dermato-Venereologica|January 1, 1990
Proliferation and differentiation of cultured epidermal cells from patients with X-linked ichthyosis and ichthyosis vulgarisP K Jensen, F H Herrmann, J Hadlich, et al.
Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Human Mutation|January 1, 1997
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophyK Wulff, J E Parrish, F H Herrmann, 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.
Acta Haematologica|January 1, 1982
The effect of diamide (azodicarboxylic acid-bis-dimethylamide) on sulfhydryl group content, proteins, and the location of phosphatidylethanolamine in human blood plateletsG Ostermann, P Spangenberg, M Meyer, 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.
Zentralblatt Fur Gynakologie|January 1, 1985
[45,X/46,X,del(Yq) sex chromosome mosaicism--analysis of the phenotypic expression]W Werner, B John, U Tuschy, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Pageof 7