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F H Herrmann

Showing results (41-50 of 66) with videos related to

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Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of haemophilia A by the polymerase chain reaction using the intragenic hind III polymorphismM Wehnert, E L Shukova, V L Surin, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1983
Proteins and glycoproteins of monkey and human platelets. Comparison by high resolution two-dimensional gel electrophoresisM Meyer, F H Herrmann, M Herrmann, et al.
Journal of Medical Genetics|March 1, 1993
Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at riskW Schröder, L Petruschka, M Wehnert, et al.
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|August 15, 1988
[Initial results of genetic carrier diagnosis in risk pedigrees with hemophilia A and B in East Germany]M Wehnert, F H Herrmann, H Metzke, et al.
Human Genetics|July 1, 1987
Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibshipsA Russo, G Barbujani, M L Mostacciuolo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2006
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 geneF H Herrmann, G Auerswald, A Ruiz-Saez, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR)M Wehnert, E L Shukova, V L Surin, et al.
Disease Markers|April 1, 1997
Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysisK Wulff, U Ebener, C S Wehnert, et al.
British Journal of Haematology|April 8, 1998
A de novo translocation 46,X,t(X;15) causing haemophilia B in a girl: a case reportW Schröder, M Poetsch, H Gazda, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Prenatal Diagnosis|August 1, 1990
Prenatal diagnosis of haemophilia A by the polymerase chain reaction using the intragenic hind III polymorphismM Wehnert, E L Shukova, V L Surin, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1983
Proteins and glycoproteins of monkey and human platelets. Comparison by high resolution two-dimensional gel electrophoresisM Meyer, F H Herrmann, M Herrmann, et al.
Journal of Medical Genetics|March 1, 1993
Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at riskW Schröder, L Petruschka, M Wehnert, et al.
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|August 15, 1988
[Initial results of genetic carrier diagnosis in risk pedigrees with hemophilia A and B in East Germany]M Wehnert, F H Herrmann, H Metzke, et al.
Human Genetics|July 1, 1987
Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibshipsA Russo, G Barbujani, M L Mostacciuolo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2006
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 geneF H Herrmann, G Auerswald, A Ruiz-Saez, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR)M Wehnert, E L Shukova, V L Surin, et al.
Disease Markers|April 1, 1997
Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysisK Wulff, U Ebener, C S Wehnert, et al.
British Journal of Haematology|April 8, 1998
A de novo translocation 46,X,t(X;15) causing haemophilia B in a girl: a case reportW Schröder, M Poetsch, H Gazda, et al.
Pageof 7