MARC details
000 -LEADER |
fixed length control field |
04750cam a2200781Ia 4500 |
001 - CONTROL NUMBER |
control field |
ocn889675195 |
003 - CONTROL NUMBER IDENTIFIER |
control field |
OCoLC |
005 - DATE AND TIME OF LATEST TRANSACTION |
control field |
20220711234218.0 |
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION |
fixed length control field |
m o d |
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION |
fixed length control field |
cr cnu---unuuu |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
fixed length control field |
140830s2015 enk ob 000 0 eng d |
040 ## - CATALOGING SOURCE |
Original cataloging agency |
EBLCP |
Language of cataloging |
eng |
Description conventions |
pn |
Transcribing agency |
EBLCP |
Modifying agency |
OCLCO |
-- |
IDEBK |
-- |
N$T |
-- |
E7B |
-- |
OCLCQ |
-- |
YDXCP |
-- |
OCLCF |
-- |
OCLCQ |
-- |
OCLCO |
-- |
OCLCQ |
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UAB |
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OCLCQ |
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OCLCA |
-- |
AU@ |
-- |
OCLCO |
-- |
OCLCA |
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AGLDB |
-- |
OCLCO |
-- |
G3B |
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IGB |
-- |
STF |
-- |
OCLCQ |
-- |
OCLCO |
020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
International Standard Book Number |
9780199383900 |
Qualifying information |
(electronic bk.) |
020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
International Standard Book Number |
0199383901 |
Qualifying information |
(electronic bk.) |
029 1# - (OCLC) |
OCLC library identifier |
AU@ |
System control number |
000053537322 |
029 1# - (OCLC) |
OCLC library identifier |
DEBBG |
System control number |
BV042794786 |
029 1# - (OCLC) |
OCLC library identifier |
AU@ |
System control number |
000062299575 |
029 1# - (OCLC) |
OCLC library identifier |
AU@ |
System control number |
000062476401 |
035 ## - SYSTEM CONTROL NUMBER |
System control number |
(OCoLC)889675195 |
050 #4 - LIBRARY OF CONGRESS CALL NUMBER |
Classification number |
RC346.4 |
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER |
Classification number |
WL 140 |
072 #7 - SUBJECT CATEGORY CODE |
Subject category code |
HEA |
Subject category code subdivision |
039000 |
Source |
bisacsh |
072 #7 - SUBJECT CATEGORY CODE |
Subject category code |
MED |
Subject category code subdivision |
014000 |
Source |
bisacsh |
072 #7 - SUBJECT CATEGORY CODE |
Subject category code |
MED |
Subject category code subdivision |
022000 |
Source |
bisacsh |
072 #7 - SUBJECT CATEGORY CODE |
Subject category code |
MED |
Subject category code subdivision |
112000 |
Source |
bisacsh |
072 #7 - SUBJECT CATEGORY CODE |
Subject category code |
MED |
Subject category code subdivision |
045000 |
Source |
bisacsh |
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER |
Classification number |
616.8/0442 |
Edition number |
23 |
049 ## - LOCAL HOLDINGS (OCLC) |
Holding library |
MAIN |
245 00 - TITLE STATEMENT |
Title |
Neurogenetics / |
Statement of responsibility, etc |
Kishor R. Kumar [and others]. |
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT) |
Place of publication, distribution, etc |
Oxford : |
Name of publisher, distributor, etc |
Oxford University Press, |
Date of publication, distribution, etc |
©2015. |
300 ## - PHYSICAL DESCRIPTION |
Extent |
1 online resource. |
336 ## - |
-- |
text |
-- |
txt |
-- |
rdacontent |
337 ## - |
-- |
computer |
-- |
c |
-- |
rdamedia |
338 ## - |
-- |
online resource |
-- |
cr |
-- |
rdacarrier |
490 1# - SERIES STATEMENT |
Series statement |
What do I do now? |
504 ## - BIBLIOGRAPHY, ETC. NOTE |
Bibliography, etc |
Includes bibliographical references. |
505 8# - FORMATTED CONTENTS NOTE |
Formatted contents note |
Machine generated contents note: 1. Early-onset dystonia -- 2. DYT5 dystonia (dopa-responsive dystonia) -- 3. Myoclonus dystonia -- 4. Paroxysmal dyskinesia -- 5. Huntington disease -- 6. Dominant Parkinson disease -- 7. Recessive Parkinson disease -- 8. Gaucher disease and Parkinson disease -- 9. Spinocerebellar ataxia type 2 -- 10. Spinocerebellar ataxia type 17 -- 11. Sialidosis -- 12. Freidreich ataxia -- 13. MELAS syndrome -- 14. MERRF -- 15. POLG-related mitochondrial disease -- 16. MNGIE syndrome -- 17. Leber hereditary optic neuropathy -- 18. Charcot-Marie-Tooth disease type -- 19. Hereditary neuropathy with liability to pressure palsy -- 20. Neurofibromatosis type 12 -- 21. The myotonic dystrophies -- 22. The dystrophinopathies -- 23. Fascioscapulohumeral dystrophy -- 24. Inclusion body myopathy with Paget disease of bone and frontotemporal dementia -- 25. Hereditary spastic paraplegia -- 26. Inherited prion diseases -- 27. Frontotemporal dementia-amyotrophic lateral sclerosis syndrome -- 28. Neurodegeneration with brain iron accumulation : other issues that may arise in patients with neurogenetic conditions -- 29. Coincidental occurrence of two monogenic disorders / Christine Klein -- 30. Direct-to-consumer genetic testing / Christine Klein -- 31. Incidental findings in genetic testing / Christine Klein. |
520 ## - SUMMARY, ETC. |
Summary, etc |
In this book, the authors use their extensive experience in the field of neurogenetics to provide readers with a practical approach for dealing with these conditions. The 31 chapters of this book cover a broad range of neurogenetic disorders, highlighting key issues with regards to the clinical assessment, diagnosis and management"--Provided by publisher. |
588 0# - |
-- |
Print version record. |
590 ## - LOCAL NOTE (RLIN) |
Local note |
eBooks on EBSCOhost |
Provenance (VM) [OBSOLETE] |
EBSCO eBook Subscription Academic Collection - Worldwide |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Nervous system |
General subdivision |
Diseases |
-- |
Genetic aspects. |
9 (RLIN) |
1024933 |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Neurogenetics. |
9 (RLIN) |
679965 |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Genetic screening. |
9 (RLIN) |
172174 |
650 12 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Nervous System Diseases |
General subdivision |
genetics |
9 (RLIN) |
1024934 |
650 22 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Genetic Testing |
9 (RLIN) |
930088 |
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Système nerveux |
General subdivision |
Maladies |
-- |
Aspect génétique. |
9 (RLIN) |
1024935 |
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Neurogénétique. |
9 (RLIN) |
944893 |
650 #6 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Dépistage génétique. |
9 (RLIN) |
930091 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
HEALTH & FITNESS |
General subdivision |
Diseases |
-- |
General. |
Source of heading or term |
bisacsh |
9 (RLIN) |
88045 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
MEDICAL |
General subdivision |
Clinical Medicine. |
Source of heading or term |
bisacsh |
9 (RLIN) |
91637 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
MEDICAL |
General subdivision |
Diseases. |
Source of heading or term |
bisacsh |
9 (RLIN) |
88037 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
MEDICAL |
General subdivision |
Evidence-Based Medicine. |
Source of heading or term |
bisacsh |
9 (RLIN) |
91638 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
MEDICAL |
General subdivision |
Internal Medicine. |
Source of heading or term |
bisacsh |
9 (RLIN) |
91639 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Nervous system |
General subdivision |
Diseases |
-- |
Genetic aspects. |
Source of heading or term |
fast |
-- |
(OCoLC)fst01036107 |
9 (RLIN) |
1024933 |
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM |
Topical term or geographic name as entry element |
Neurogenetics. |
Source of heading or term |
fast |
-- |
(OCoLC)fst01036353 |
9 (RLIN) |
679965 |
655 #4 - INDEX TERM--GENRE/FORM |
Genre/form data or focus term |
Electronic books. |
700 1# - ADDED ENTRY--PERSONAL NAME |
Personal name |
Kumar, Kishore R. |
9 (RLIN) |
1024936 |
776 08 - ADDITIONAL PHYSICAL FORM ENTRY |
Display text |
Print version: |
Title |
Neurogenetics. |
Place, publisher, and date of publication |
Oxford : Oxford University Press, ©2015 |
International Standard Book Number |
9780199383894 |
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE |
Uniform title |
What do I do now? |
9 (RLIN) |
217805 |
856 40 - ELECTRONIC LOCATION AND ACCESS |
Uniform Resource Identifier |
<a href="https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=835599">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=835599</a> |
938 ## - |
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ProQuest Ebook Central |
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EBLB |
-- |
EBL1771652 |
938 ## - |
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ebrary |
-- |
EBRY |
-- |
ebr10915733 |
938 ## - |
-- |
EBSCOhost |
-- |
EBSC |
-- |
835599 |
938 ## - |
-- |
ProQuest MyiLibrary Digital eBook Collection |
-- |
IDEB |
-- |
cis29660600 |
938 ## - |
-- |
YBP Library Services |
-- |
YANK |
-- |
12048365 |
938 ## - |
-- |
YBP Library Services |
-- |
YANK |
-- |
12890653 |
994 ## - |
-- |
92 |
-- |
INOPJ |