FSHD facioscapulohumeral muscular dystrophy : clinical medicine and molecular cell biology /
| Other Authors: | , |
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| Format: | Book |
| Language: | English French |
| Published: |
London ; New York :
BIOS Scientific Publishers,
2004.
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| Subjects: |
Table of Contents:
- Introduction and overview of FSHD / M. Upadhyaya, D.N. Cooper
- Facioscapulohumeral muscular dystrophy: historical background and literature review / M. Rogers
- Facioscapulohumeral muscular dystrophy: a clinician's experience / G.W. Padberg
- Mapping of the FSHD gene and the discovery of the pathognomonic deletion / R.R. Frants ... [et al.]
- Identification and characterization of candidate genes in FSHD region / S. van Koningsbruggen, R.R. Frants, S.M. van der Maarel
- Evolution and structural organization of the homeobox-containing repeat D4Z4 / J.E. Hewitt
- Subtelomeric exchange between 4q and 10q sequences / R.R. Frants, S.M. van der Maarel
- Genomic analysis of the subtelomeric regions of human chromosomes 10q and 4q: relevance to FSHD / M. van Geel, J.E. Hewitt
- The DUX gene family and FSHD / F. Coppie ... [et al.]
- Facioscapulohumeral muscular dystrophy (FSHD) : a disorder of muscle gene repression / R. Tupler, D. Gabellini
- Genotype-phenotype relationships in FSHD / P. Lunt, M. Upadhyaya, M.C. Koch
- Mosaicism and FSHD / P.G.M. van Overveld, R.R. Frants, S.M. van der Maarel
- Retinal vascular abnormalities in FSHD : a therapeutic message; clues to pathogenesis / R.B. Fitzsimons
- Unusual clinical features associated with FSHD / Y.K. Hayashi
- Molecular diagnosis of FSHD / R.J.L.F. Lemmers ... [et al.]
- FSHD myoblasts: in vitro studies / D.A. Figlewicz ... [et al.]
- Exploring hypotheses about the molecular aetiology of FSHD : loss of heterochromatin spreading and other long-range interaction models / M. Ehrlich
- Histological, immunological, molecular, and ultrastructural characteristics of FSHD muscle / M.T. Rogers, M. Upadhyaya, C.A. Sewry
- Linkage analysis in non-chromosome 4-linked FSHD / K. Bastress ... [et al.]
- Facioscapulohumeral muscular dystrophy : gender differences and genetic counselling in a complex disorder / M. Manuela de Oliveira Tonini, M. Zatz
- Genetic counselling for facioscapulohumeral muscular dystrophy (FSHD) / P. Lunt
- Sarcolemmal reorganization in FSHD / P. Reed ... [et al.]
- Expression profiling in FSHD / S.T. Winokur, Y.-W. Chen
- Therapeutic trials and medical management in FSHD / R. Tawil, R.C. Griggs