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F H Herrmann

Showing results (1-10 of 66) with videos related to

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Dermatologische Monatschrift|January 1, 1989
[The genetics and molecular genetics of X-chromosomal recessive ichthyosis]F H Herrmann
Clinical Genetics|September 1, 1984
Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocationW Werner, F H Herrmann
Journal of Inherited Metabolic Disease|January 1, 1990
Characterization of three new deletions at the 5' end of the HPRT structural geneM Wehnert, F H Herrmann
Human Mutation|June 22, 2000
Twenty two novel mutations of the factor VII gene in factor VII deficiencyK Wulff, F H Herrmann
Hamostaseologie|May 12, 2004
[Factors VII, VIII, IX, and X: molecular genetics and gene diagnosis]F H Herrmann, K Wulff
Thrombosis and Haemostasis|October 30, 1985
Diversity of glycoprotein deficiencies in Glanzmann's thrombastheniaM Meyer, F H Herrmann
Journal of the Neurological Sciences|December 1, 1983
Carrier detection in X-linked Becker muscular dystrophy by muscle provocation test (MPT)F H Herrmann, A W Spiegler
Journal of Inherited Metabolic Disease|January 1, 1987
Arylsulphatase C activity in leukocytes of patients and carriers of X-linked ichthyosisF H Herrmann, U Grimm, J Hadlich
Clinical Genetics|January 1, 1990
RFLP analysis for diagnosis of haemophilia A in the German Democratic RepublicF H Herrmann, M Wehnert, K Wulff
Human Genetics|November 1, 1990
A new marker at DXS 115 useful for carrier detection in hemophilia AM Wehnert, W Schröder, F H Herrmann
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Dermatologische Monatschrift|January 1, 1989
[The genetics and molecular genetics of X-chromosomal recessive ichthyosis]F H Herrmann
Clinical Genetics|September 1, 1984
Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocationW Werner, F H Herrmann
Journal of Inherited Metabolic Disease|January 1, 1990
Characterization of three new deletions at the 5' end of the HPRT structural geneM Wehnert, F H Herrmann
Human Mutation|June 22, 2000
Twenty two novel mutations of the factor VII gene in factor VII deficiencyK Wulff, F H Herrmann
Hamostaseologie|May 12, 2004
[Factors VII, VIII, IX, and X: molecular genetics and gene diagnosis]F H Herrmann, K Wulff
Thrombosis and Haemostasis|October 30, 1985
Diversity of glycoprotein deficiencies in Glanzmann's thrombastheniaM Meyer, F H Herrmann
Journal of the Neurological Sciences|December 1, 1983
Carrier detection in X-linked Becker muscular dystrophy by muscle provocation test (MPT)F H Herrmann, A W Spiegler
Journal of Inherited Metabolic Disease|January 1, 1987
Arylsulphatase C activity in leukocytes of patients and carriers of X-linked ichthyosisF H Herrmann, U Grimm, J Hadlich
Clinical Genetics|January 1, 1990
RFLP analysis for diagnosis of haemophilia A in the German Democratic RepublicF H Herrmann, M Wehnert, K Wulff
Human Genetics|November 1, 1990
A new marker at DXS 115 useful for carrier detection in hemophilia AM Wehnert, W Schröder, F H Herrmann
Pageof 7