The Wills Eye handbook of ocular genetics (Record no. 92953)

MARC details
000 -LEADER
fixed length control field 05378cam a22006138i 4500
001 - CONTROL NUMBER
control field on1000150685
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20221128213402.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
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008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170807s2018 nyua obf 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2017037367
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
019 ## -
-- 1051040759
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781626232945
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1626232946
Qualifying information (electronic bk.)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9781626232938
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 1626232938
035 ## - SYSTEM CONTROL NUMBER
System control number 1664770
-- (N$T)
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)1000150685
Canceled/invalid control number (OCoLC)1051040759
042 ## - AUTHENTICATION CODE
Authentication code pcc
060 10 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WW 140
060 #4 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER
Classification number WW 39
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 085000
Source bisacsh
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
100 1# - MAIN ENTRY--PERSONAL NAME
Personal author Levin, Alex V.,
Relator term author.
245 14 - TITLE STATEMENT
Title The Wills Eye handbook of ocular genetics
Statement of responsibility, etc
Medium [E-Book]
246 3# - VARIANT TITLE
Title Handbook of ocular genetics
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture New York :
Name of producer, publisher, distributor, manufacturer Thieme,
Date of production, publication, distribution, manufacture, or copyright notice [2018]
300 ## - PHYSICAL DESCRIPTION
Physical description 1 online resource :
Other physical details illustrations
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
336 ## - CONTENT TYPE
Content type term still image
Content type code sti
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index
505 0# - CONTENTS
Contents Basic Genetics -- Inheritance Patterns -- Genetic Testing -- Ethical Issues -- Corneal Dystrophies - Aniridia -- Peters Anomaly -- Axenfeld-Rieger Syndrome -- Primary Congenital Glaucoma and Juvenile Open Angle Glaucoma -- Childhood Cataract - Microphthalmia -- Marfan Syndrome and Other Causes of Ectopia Lentis -- Familial Exudative Vitreoretinopathy -- Stickler Syndrome -- VCAN Vitreoretinopathies (Erosive Vitreoretinopathy and Wagner Syndrome) -- Incontinentia Pigmenti -- Retinitis Pigmentosa -- Usher Syndrome -- Bardet-Biedl Syndrome -- Cone-Rod Dystrophy - Choroideremia -- Enhanced S-Cone Syndrome and Other NR2E3-Related Retinal Dystrophies -- Stargardt Disease and Other ABCA4 Retinopathies -- Best Vitelliform Macular Dystrophy (Best Disease) -- Leber Congenital Amaurosis - Achromatopsia -- Congenital Stationary Night Blindness -- Juvenile X-Linked Retinoschisis - Retinoblastoma -- Optic Nerve Hypoplasia -- Leber Hereditary Optic Neuropathy -- Complex Ocular Disorders - Albinism.
520 ## - ABSTRACT
Abstract "Many serious, potentially blinding eye disorders have a genetic basis. Currently, there are relatively few ocular geneticists in the world, yet inherited eye disease is one of the leading causes of blindness worldwide. Significant strides have been made in gene identification and acquisition of knowledge on the underlying mechanisms of hereditary eye disease. The field of ocular genetics is becoming an increasingly relevant part of ophthalmologists'purview. This has resulted in a dire need for a comprehensive textbook ophthalmologists and other professionals who work with patients with genetic disorders can utilize to gain a better understanding of inherited eye disorders.The Wills Eye Handbook of Ocular Genetics, by Alex Levin, Mario Zanolli, and Jenina Capasso of Wills Eye Hospital, is a practical, reader-friendly guide on the diagnosis and management of ophthalmic genetic conditions. Every chapter begins with a disease overview, followed by relevant modern genetic concepts, pathways to attaining the correct diagnosis, and pitfalls and pearls gleaned from years of hands-on expertise. At the end of each chapter, questions and answers enable readers to test their knowledge in real-life scenarios they might face in everyday practice. The ultimate goal of this clinically robust handbook is to facilitate optimal patient management and outcomes.Key FeaturesFundamentals, including basic genetics, inheritance patterns, genetic testing, and ethical issuesPatient-centered genetic counseling issues such as reproduction, dealing with emotional reactions, prognosis, and future optionsAnterior segment disorders - from corneal dystrophies and aniridia - to childhood cataract and microphthalmiaA broad spectrum of vitreoretinopathies and retinal diseases including incontinentia pigmenti, retinitis pigmentosa, Bardet-Biedl syndrome, choroideremia, Stargardt disease, achromatopsia, and juvenile X-linked retinoschisisThis textbook is essential reading for practitioners at all levels and in all subspecialties including ophthalmology and genetics. They will find it an excellent resource for navigating the complexities of genetic eye disease."--Publisher.
590 ## - LOCAL NOTE (RLIN)
Local note Master record variable field(s) change: 650
650 #0 - SUBJECT HEADINGS
Subject term Eye
General subdivision Diseases
-- Genetics
650 #0 - SUBJECT HEADINGS
Subject term Eye
General subdivision Diseases.
650 #0 - SUBJECT HEADINGS
Subject term Genetic diseases and disorders.
650 #2 - SUBJECT HEADINGS
Subject term Eye Diseases, Hereditary
General subdivision genetics.
650 #2 - SUBJECT HEADINGS
Subject term Eye Diseases, Hereditary
General subdivision therapy.
700 1# - ADDED PERSONAL NAME
Added personal author Zanolli, Mario,
Relator term author.
700 1# - ADDED PERSONAL NAME
Added personal author Capasso, Jenina,
Relator term author.
710 2# - ADDED CORPORATE NAME
Added corporate author Wills Eye Hospital (Philadelphia, Pa.)
856 40 - ONLINE RESOURCE
Uniform Resource Identifier <a href="https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1664770">https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1664770</a>
Link text Kingston Hospital NHS Foundation Trust OpenAthens account holders click here for access
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Suppress in OPAC Do not Suppress in OPAC
263 ## - PROJECTED PUBLICATION DATE
Projected publication date 1804
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Description based on print version record
938 ## -
-- EBSCOhost
-- EBSC
-- 1664770
938 ## -
-- YBP Library Services
-- YANK
-- 15064137
994 ## -
-- 92
-- N$T
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Shelving location Date acquired Source of acquisition Total Checkouts Date last seen Uniform Resource Identifier Price effective from Koha item type
        Stenhouse Library Stenhouse Library   28/11/2022 eBook EBSCO clinical collection   28/11/2022 https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=1664770 28/11/2022 Electronic book
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