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02721nam a22003015i 4500 |
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978-1-59259-138-1 |
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20191026231928.0 |
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cr nn 008mamaa |
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100301s2001 xxu| s |||| 0|eng d |
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|a 9781592591381
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7 |
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|a 10.1385/1592591388
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
1 |
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|a Muscular Dystrophy
|b Methods and Protocols /
|c edited by Katherine M.D. Bushby, Louise V.B. Anderson.
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| 250 |
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|a 1st ed. 2001.
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| 260 |
# |
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|a Totowa, NJ :
|b Humana Press :
|b Imprint: Humana,
|c 2001.
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| 300 |
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|a XII, 458 p.
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 490 |
1 |
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|a Methods in Molecular Medicine,
|v 43
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| 505 |
0 |
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|a Background -- Application of Molecular Methodologies in Muscular Dystrophies -- Clinical Examination as a Tool for Diagnosis -- Histopathological Diagnosis of Muscular Dystrophies -- Serum Creatine Kinase in Progressive Muscular Dystrophies -- The molecular approach -- Deletion and Duplication Analysis in Males Affected with Duchenne or Becker Muscular Dystrophy -- Point Mutation Detection in the Dystrophin Gene -- DNA-Based Techniques for Detection of Carriers of Duchenne and Becker Muscular Dystrophy -- Fluorescence In Situ Hybridization Analysis for Carrier Detection in Duchenne/Becker Muscular Dystrophy -- DNA- Based Prenatal Diagnosis for Duchenne and Becker Muscular Dystrophy -- Molecular Diagnosis and Genetic Counseling of the Manifesting Carrier of Duchenne Muscular Dystrophy -- Mutation Analysis of X-Linked Emery-Dreifuss Muscular Dystrophy Gene -- Analysis of LAMA2 Gene in Merosin- Deficient Congenital Dystrophy -- ?-Sarcoglycan Mutations -- Mutation Detection in ?- and ?-Sarcoglycan (LGMD2E and LGMD2C) -- Mutation Analysis in ?-Sarcoglycan (LGMD2F) -- Molecular Diagnosis of Calpainopathies -- Molecular Investigation of LGMD2B-Haplotype Analysis and Mutation Screening -- Molecular Analysis of Facioscapulohumeral Muscular Dystrophy (FSHD1) -- Protein Analysis in the Muscular Dystrophies -- Analysis of Protein Expression in Muscular Dystrophies -- Immunological Reagents and Amplification Systems -- Immunocytochemical Analysis -- Multiplex Western Blot Analysis of Muscular Dystrophy Proteins -- Fetal Muscle Biopsy -- Use of Animal Models to Understand Human Muscular Dystrophy -- Options for Development of Gene-Based Therapy for Muscular Dystrophy.
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| 650 |
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|a Neurology .
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| 650 |
1 |
4 |
|a Neurology.
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| 700 |
1 |
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|a Bushby, Katherine M.D.
|e editor.
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| 700 |
1 |
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|a Anderson, Louise V.B.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 856 |
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|u https://doi.org/10.1385/1592591388
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