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• 2004003241 contributor B9808544.
• 2004003241 created "2004.".
• 2004003241 date "2004".
• 2004003241 date "2004.".
• 2004003241 dateCopyrighted "2004.".
• 2004003241 description "Includes bibliographical references and index.".
• 2004003241 description "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.".
• 2004003241 extent "xix, 392 p. :".
• 2004003241 identifier "1859962440".
• 2004003241 identifier es0804_4062.html.
• 2004003241 identifier 2004003241-d.html.
• 2004003241 identifier 2004003241.html.
• 2004003241 issued "2004".
• 2004003241 issued "2004.".
• 2004003241 language "eng".
• 2004003241 publisher "London ; New York : BIOS Scientific Publishers,".
• 2004003241 subject "616.7/48 22".
• 2004003241 subject "Facioscapulohumeral muscular dystrophy.".
• 2004003241 subject "RC935.M7 F74 2004".
• 2004003241 tableOfContents "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.".
• 2004003241 title "FSHD facioscapulohumeral muscular dystrophy : clinical medicine and molecular cell biology / edited by Meena Upadhyaya and David N Cooper.".
• 2004003241 type "text".