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M C Koch

Showing results (11-20 of 59) with videos related to

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Human Molecular Genetics|June 1, 1994
A recurrent 14 bp deletion in the CLCN1 gene associated with generalized myotonia (Becker)C Meyer-Kleine, K Ricker, M Otto, et al.
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
Muscle & Nerve|June 1, 1994
Mixed axonal-demyelinating polyneuropathy as predominant manifestation of myotonic dystrophyH J von Giesen, G Stoll, M C Koch, et al.
Human Genetics|October 1, 1996
Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesisJ Köhler, B Rupilius, M Otto, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 1998
The molecular genetic approach to "Bartter's syndrome"L Károlyi, M C Koch, K H Grzeschik, et al.
European Journal of Pediatrics|July 17, 1998
Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida populationM C Koch, K Stegmann, A Ziegler, et al.
The EMBO Journal|February 15, 1994
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)K Steinmeyer, C Lorenz, M Pusch, et al.
Mutation Research|September 10, 1999
Human transcription factor SLUG: mutation analysis in patients with neural tube defects and identification of a missense mutation (D119E) in the Slug subfamily-defining regionK Stegmann, J Boecker, C Kosan, et al.
Human Molecular Genetics|June 1, 1994
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotoniaC Lorenz, C Meyer-Kleine, K Steinmeyer, et al.
Zeitschrift Fur Kardiologie|May 4, 2005
[Facioscapulohumeral muscle dystrophy and heart disease]P Emmrich, V Ogunlade, T Gradistanac, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|June 1, 1994
A recurrent 14 bp deletion in the CLCN1 gene associated with generalized myotonia (Becker)C Meyer-Kleine, K Ricker, M Otto, et al.
American Journal of Human Genetics|June 1, 1991
Genetic risks for children of women with myotonic dystrophyM C Koch, T Grimm, H G Harley, et al.
Muscle & Nerve|June 1, 1994
Mixed axonal-demyelinating polyneuropathy as predominant manifestation of myotonic dystrophyH J von Giesen, G Stoll, M C Koch, et al.
Human Genetics|October 1, 1996
Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesisJ Köhler, B Rupilius, M Otto, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 20, 1998
The molecular genetic approach to "Bartter's syndrome"L Károlyi, M C Koch, K H Grzeschik, et al.
European Journal of Pediatrics|July 17, 1998
Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida populationM C Koch, K Stegmann, A Ziegler, et al.
The EMBO Journal|February 15, 1994
Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)K Steinmeyer, C Lorenz, M Pusch, et al.
Mutation Research|September 10, 1999
Human transcription factor SLUG: mutation analysis in patients with neural tube defects and identification of a missense mutation (D119E) in the Slug subfamily-defining regionK Stegmann, J Boecker, C Kosan, et al.
Human Molecular Genetics|June 1, 1994
Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotoniaC Lorenz, C Meyer-Kleine, K Steinmeyer, et al.
Zeitschrift Fur Kardiologie|May 4, 2005
[Facioscapulohumeral muscle dystrophy and heart disease]P Emmrich, V Ogunlade, T Gradistanac, et al.
Pageof 6