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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 dystrophy
M C Koch, T Grimm, H G Harley, et al.
Muscle & Nerve
|
June 1, 1994
Mixed axonal-demyelinating polyneuropathy as predominant manifestation of myotonic dystrophy
H 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 oogenesis
J 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 population
M 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 region
K 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 myotonia
C 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.
Page
of 6
Search research articles
Search
Showing results (11-20 of 59) with videos related to
Sort By:
Page
of 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 dystrophy
M C Koch, T Grimm, H G Harley, et al.
Muscle & Nerve
|
June 1, 1994
Mixed axonal-demyelinating polyneuropathy as predominant manifestation of myotonic dystrophy
H 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 oogenesis
J 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 population
M 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 region
K 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 myotonia
C 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.
Page
of 6