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F H Herrmann

Showing results (11-20 of 66) with videos related to

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Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Genomic diagnosis of haemophilia A and B in the German Democratic RepublicF H Herrmann, M Wehnert, W Schröder
Disease Markers|April 1, 1989
Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia AM Wehnert, F H Herrmann, K Wulff
Haemostasis|January 1, 1982
Protein and glycoprotein abnormalities in an unusual subtype of Glanzmann's thrombastheniaF H Herrmann, M Meyer, E Ihle
Journal of Neurology|January 1, 1985
Becker muscular dystrophy: carrier detection by real-time ultrasoundA W Spiegler, S Schindler, F H Herrmann
Histopathology|April 27, 1999
Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinomaM Poetsch, B Kleist, G Lorenz, et al.
Acta Biochimica Polonica|March 4, 2000
Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX geneK Wulff, K Bykowska, S Lopaciuk, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 13, 1990
The immunological evidence for a phenylalanine hydroxylase like immunoreactive protein in different human cells and tissuesL Petruschka, I Rebrin, U Grimm, et al.
Thrombosis and Haemostasis|January 4, 1998
Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomesW Schröder, K Wulff, K Wollina, et al.
European Journal of Pediatrics|January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56aF H Herrmann, K Wulff, M Schütz, et al.
Journal of Neurology|December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Genomic diagnosis of haemophilia A and B in the German Democratic RepublicF H Herrmann, M Wehnert, W Schröder
Disease Markers|April 1, 1989
Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia AM Wehnert, F H Herrmann, K Wulff
Haemostasis|January 1, 1982
Protein and glycoprotein abnormalities in an unusual subtype of Glanzmann's thrombastheniaF H Herrmann, M Meyer, E Ihle
Journal of Neurology|January 1, 1985
Becker muscular dystrophy: carrier detection by real-time ultrasoundA W Spiegler, S Schindler, F H Herrmann
Histopathology|April 27, 1999
Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinomaM Poetsch, B Kleist, G Lorenz, et al.
Acta Biochimica Polonica|March 4, 2000
Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX geneK Wulff, K Bykowska, S Lopaciuk, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 13, 1990
The immunological evidence for a phenylalanine hydroxylase like immunoreactive protein in different human cells and tissuesL Petruschka, I Rebrin, U Grimm, et al.
Thrombosis and Haemostasis|January 4, 1998
Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomesW Schröder, K Wulff, K Wollina, et al.
European Journal of Pediatrics|January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56aF H Herrmann, K Wulff, M Schütz, et al.
Journal of Neurology|December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.
Pageof 7