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Second Indicator |
Subfields |
| LEADER |
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| 001 |
in00004499413 |
| 005 |
20191203131239.0 |
| 008 |
040211s2004 enka b 001 0 eng |
| 010 |
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|a 2004003241
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| 016 |
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|2 DNLM
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|d UtOrBLW
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| 041 |
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|a eng
|a fre
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| 042 |
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|a pcc
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| 049 |
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|a TMVM
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| 050 |
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|a RC935.M7
|b F74 2004
|
| 060 |
0 |
0 |
|a 2004 F-828
|
| 060 |
1 |
0 |
|a WE 559
|b F948 2004
|
| 060 |
|
4 |
|a WE 559
|b F948 2004
|
| 082 |
0 |
0 |
|a 616.7/48
|2 22
|
| 245 |
0 |
0 |
|a FSHD facioscapulohumeral muscular dystrophy :
|b clinical medicine and molecular cell biology /
|c edited by Meena Upadhyaya and David N Cooper.
|
| 264 |
|
1 |
|a London ;
|a New York :
|b BIOS Scientific Publishers,
|c 2004.
|
| 300 |
|
|
|a xix, 392 pages :
|b illustrations ;
|c 24 cm.
|
| 336 |
|
|
|a text
|2 rdacontent
|b txt
|
| 337 |
|
|
|a unmediated
|2 rdamedia
|
| 338 |
|
|
|a volume
|2 rdacarrier
|b nc
|
| 504 |
|
|
|a Includes bibliographical references and index.
|
| 505 |
0 |
|
|a 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
|
| 650 |
|
2 |
|a Muscular Dystrophy, Facioscapulohumeral
|x genetics.
|
| 650 |
|
2 |
|a Genetic Techniques.
|
| 700 |
1 |
|
|a Upadhyaya, M.
|q (Meena)
|
| 700 |
1 |
|
|a Cooper, David N.
|q (David Neil),
|d 1957-
|
| 948 |
|
|
|a PO 8951
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| 999 |
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|a MARS
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|t 0
|
| 952 |
f |
f |
|p normal
|a Texas A&M University
|b College Station
|c Medical Sciences Library
|s MSL Book Stacks
|d MSL: Book Stacks
|t 0
|e WE 559 F948 2004
|h National Library of Medicine classification
|i unmediated -- volume
|m 3238901875339
|
| 998 |
f |
f |
|a WE 559 F948 2004
|t 0
|l MSL: Book Stacks
|