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C R Müller

Showing results (41-50 of 143) with videos related to

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Journal of Neurology|December 1, 1990
Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in manR Gold, B Meurers, H Reichmann, et al.
Journal of Supramolecular Structure|January 1, 1977
Isolation and purification of bacterial membrane proteins by the use of organic solvents: the lactose permease and the carbodiimide-reactive protein of the adenosinetriphosphatase complex of Escherichia coliK Altendorf, M Lukas, B Kohl, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2013
Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene--a case reportS Rost, V Aumann, I Nanda, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Detection of large duplications within the factor VIII gene by MLPAS Rost, S Löffler, A Pavlova, et al.
Journal of Neurology|March 1, 1994
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophyR Gold, W Kress, T Bettecken, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Parental source effect on inherited mutations in the dystrophin gene of mice and humansW Kress, T Grimm, C R Müller, et al.
Der Nervenarzt|June 1, 1991
[Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]R Gold, W Kress, B Meurers, et al.
Cytogenetics and Cell Genetics|January 1, 1996
A complex satellite DNA polymorphism flanking the human ryanodine receptor gene (RYR1)W Wolz, U Wendelmuth, S Rouquier, et al.
The European Physical Journal. E, Soft Matter|September 25, 2012
On the occurrence of polygon-shaped patterns in vibrated cylindrical granular bedsG Lu, J R Third, M H Köhl, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.
Pageof 15

Showing results (41-50 of 143) with videos related to

Sort By:
Pageof 15
Journal of Neurology|December 1, 1990
Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in manR Gold, B Meurers, H Reichmann, et al.
Journal of Supramolecular Structure|January 1, 1977
Isolation and purification of bacterial membrane proteins by the use of organic solvents: the lactose permease and the carbodiimide-reactive protein of the adenosinetriphosphatase complex of Escherichia coliK Altendorf, M Lukas, B Kohl, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2013
Mild haemophilia A in a female patient with a large X-chromosomal deletion and a missense mutation in the F8 gene--a case reportS Rost, V Aumann, I Nanda, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Detection of large duplications within the factor VIII gene by MLPAS Rost, S Löffler, A Pavlova, et al.
Journal of Neurology|March 1, 1994
A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophyR Gold, W Kress, T Bettecken, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Parental source effect on inherited mutations in the dystrophin gene of mice and humansW Kress, T Grimm, C R Müller, et al.
Der Nervenarzt|June 1, 1991
[Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]R Gold, W Kress, B Meurers, et al.
Cytogenetics and Cell Genetics|January 1, 1996
A complex satellite DNA polymorphism flanking the human ryanodine receptor gene (RYR1)W Wolz, U Wendelmuth, S Rouquier, et al.
The European Physical Journal. E, Soft Matter|September 25, 2012
On the occurrence of polygon-shaped patterns in vibrated cylindrical granular bedsG Lu, J R Third, M H Köhl, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)C Schneider, T Grimm, W Kress, et al.
Pageof 15