खोज परिणाम - C. R. Müller

  • प्रदर्शित 1 - 6 परिणाम 6
परिणाम को परिष्कृत करें
  1. 1
    On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.

    On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis. द्वारा T. Grimm, Gerhard Meng, Sabina Liechti‐Gallati, T. Bettecken, C R Müller, B. Müller

    प्रकाशित 1994
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  2. 2
    Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment

    Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment द्वारा Matthias Watzka, Christof Geisen, Carville G. Bevans, Katja Sittinger, Gabriele Spohn, Simone Rost, E. Seifried, C. R. Müller, Johannes Oldenburg

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  3. 3
    Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group

    Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group द्वारा Klaus P.E. Glahn, F.R. ELLIS, P.J. Halsall, C. R. Müller, M.M.J. Snoeck, A. Urwyler, Frank Wappler

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  4. 4
    European Malignant Hyperthermia Group guidelines for investigation of malignant hyperthermia susceptibility

    European Malignant Hyperthermia Group guidelines for investigation of malignant hyperthermia susceptibility द्वारा Philip M. Hopkins, Henrik Rüffert, M.M.J. Snoeck, Thierry Girard, Klaus P.E. Glahn, F.R. ELLIS, C. R. Müller, A. Urwyler

    प्रकाशित 2015
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    Artigo
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    में बचाया:
  5. 5
    Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

    Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies द्वारा Haiyan Zhou, Heinz Jungbluth, C. Sewry, Longhua Feng, Enrico Bertini, K. Bushby, Volker Straub, H. Roper, Michael R. Rose, Martin Brockington, Maria Kinali, Adnan Manzur, S. Robb, Richard Appleton, Sonia Messina, Adele D'Amico, Rosaline C. M. Quinlivan, Michael Swash, C. R. Müller, S. Brown, Susan Treves, Francesco Muntoni

    प्रकाशित 2007
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    Artigo
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    में बचाया:
  6. 6
    <i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei

    <i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei द्वारा Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou, Komala Pillay, Heather Henderson, Wolfram Kreß, C. R. Müller, Alvin Ndondo, V. Cloke, Thomas Cullup, Enrico Bertini, C. Boennemann, Volker Straub, Rosaline C. M. Quinlivan, James J. Dowling, Safa Al Sarraj, Susan Treves, Stephen Abbs, Adnan Y. Manzur, Caroline A. Sewry, Francesco Muntoni, Heinz Jungbluth

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:

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