FSHD facioscapulohumeral muscular dystrophy [electronic resource] : clinical medicine and molecular cell biology / edited by Meena Upadhyaya and David N. Cooper.
Publication details: London ; New York : BIOS Scientific Publishers, 2004.Description: xix, 392 p. : illISBN:- 9780203483671
- Also available in print edition. CRC Press (http://www.crcpress.com)
eBooks
Includes bibliographical references and index.
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.
Also available in print edition. CRC Press (http://www.crcpress.com)
Mode of access: World Wide Web.