FSHD: facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology
Gespeichert in:
| Format: | Buch |
|---|---|
| Sprache: | English |
| Veröffentlicht: |
New York, NY [u.a.]
Taylor & Francis
2006
|
| Ausgabe: | 1. publ., transferred to digital print. |
| Schlagworte: | |
| Online-Zugang: | Table of contents Book review (E-STREAMS) Inhaltsverzeichnis |
| Beschreibung: | Nebent.: Facioscapulohumeral muscular dystrophy |
| Beschreibung: | XIX, 392 S. Ill., graph. Darst. |
| ISBN: | 1859962440 |
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| 246 | 1 | 3 | |a Facioscapulohumeral muscular dystrophy |
| 250 | |a 1. publ., transferred to digital print. | ||
| 264 | 1 | |a New York, NY [u.a.] |b Taylor & Francis |c 2006 | |
| 300 | |a XIX, 392 S. |b Ill., graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
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Datensatz im Suchindex
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| adam_text | FSHD FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY / UPADHYAYA, MEENA : 2004
TABLE OF CONTENTS / INHALTSVERZEICHNIS
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.
DIESES SCHRIFTSTUECK WURDE MASCHINELL ERZEUGT.
|
| adam_txt |
FSHD FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY / UPADHYAYA, MEENA : 2004
TABLE OF CONTENTS / INHALTSVERZEICHNIS
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.
DIESES SCHRIFTSTUECK WURDE MASCHINELL ERZEUGT. |
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| language | English |
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| spelling | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology ed. by Meena Upadhyaya ... Facioscapulohumeral muscular dystrophy 1. publ., transferred to digital print. New York, NY [u.a.] Taylor & Francis 2006 XIX, 392 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Nebent.: Facioscapulohumeral muscular dystrophy Landouzy-Déjerine-Atrophie (DE-588)4419492-4 gnd rswk-swf Landouzy-Déjerine-Atrophie (DE-588)4419492-4 s b DE-604 Upadhyaya, Meena Sonstige oth http://www.loc.gov/catdir/toc/ecip0415/2004003241.html Table of contents http://www.e-streams.com/es0804/es0804_4062.html Book review (E-STREAMS) LoC Fremddatenuebernahme application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=014788488&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology Facioscapulohumeral muscular dystrophy Landouzy-Déjerine-Atrophie (DE-588)4419492-4 gnd |
| subject_GND | (DE-588)4419492-4 |
| title | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology |
| title_alt | Facioscapulohumeral muscular dystrophy |
| title_auth | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology |
| title_exact_search | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology |
| title_exact_search_txtP | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology |
| title_full | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology ed. by Meena Upadhyaya ... |
| title_fullStr | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology ed. by Meena Upadhyaya ... |
| title_full_unstemmed | FSHD facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology ed. by Meena Upadhyaya ... |
| title_short | FSHD |
| title_sort | fshd facioscapulohumeral muscular dystrophy clinical medicine and molecular cell biology |
| title_sub | facioscapulohumeral muscular dystrophy ; clinical medicine and molecular cell biology |
| topic | Facioscapulohumeral muscular dystrophy Landouzy-Déjerine-Atrophie (DE-588)4419492-4 gnd |
| topic_facet | Facioscapulohumeral muscular dystrophy Landouzy-Déjerine-Atrophie |
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