Emery's Elements of Medical Genetics and Genomics (Record no. 49313)
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fixed length control field | 02280nam a2200181 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20230222171320.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
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020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
International Standard Book Number | 9780702079665 |
100 ## - MAIN ENTRY--PERSONAL NAME | |
Personal name | <a href="Turnpenny, Peter D">Turnpenny, Peter D</a> |
245 ## - TITLE STATEMENT | |
Title | Emery's Elements of Medical Genetics and Genomics |
250 ## - EDITION STATEMENT | |
Edition statement | 16 |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | Elsevier Health Sciences |
Date of publication, distribution, etc. | 2017 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 435 p. |
500 ## - GENERAL NOTE | |
General note | Long recognized as a leading textbook in this fast-moving field, Emery's Elements of Medical Genetics and Genomics offers current, complete information with a strong basis in practical clinical genetics and genomics for medical school and beyond. The 16th Edition of this award-winning text has been thoroughly updated throughout and includes case-based and multiple-choice questions, end-of-chapter summaries, an extensive glossary, and convenient online access, making it an ideal choice for all medical undergraduates as well as postgraduates seeking to improve their understanding and knowledge.<br/>Table of Contents<br/>1 The History and Impact of Genetics in Medicine<br/><br/>Section A: The Scientific Basis of Human Genetics<br/><br/>2 The Cellular and Molecular Basis of Inheritance<br/><br/>3 Chromosomes and Cell Division<br/><br/>4 Finding the Cause of Monogenic Disorders by Identifying Disease Genes<br/><br/>5 Laboratory Techniques for Diagnosis of Monogenic Disorders<br/><br/>6 Patterns of Inheritance<br/><br/>7 Population and Mathematical Genetics<br/><br/>8 Risk Calculation<br/><br/>9 Developmental Genetics<br/><br/>Section B: Genetics in Medicine and Genomic Medicine<br/><br/>10 Common Disease, Polygenic and Multifactorial Genetics<br/><br/>11 Screening for Genetic Disease<br/><br/>12 Haemoglobin and the Haemoglobinopathies<br/><br/>13 Immunogenetics<br/><br/>14 The Genetics of Cancer and Cancer Genetics<br/><br/>15 Pharmacogenomics, Precision Medicine and the Treatment of Genetic Disease<br/><br/>Section C: Clinical Genetics, Counselling and Ethics<br/><br/>16 Congenital Abnormalities, Dysmorphic Syndromes and Intellectual Disability<br/><br/>17 Chromosome Disorders<br/><br/>18 Inborn Errors of Metabolism<br/><br/>19 Mainstream Monogenic Disorders<br/><br/>20 Prenatal Testing and Reproductive Genetics<br/><br/>21 Genetic Counselling<br/><br/>22 Ethical and Legal Issues in Medical Genetics |
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Medical Genetics; Human Genetics; Genomics |
700 ## - ADDED ENTRY--PERSONAL NAME | |
Personal name | Ellard, Sian; Cleaver, Ruth |
942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
Source of classification or shelving scheme | |
Koha item type | Books |
Withdrawn status | Lost status | Damaged status | Not for loan | Home library | Current library | Shelving location | Full call number | Barcode | Date last seen | Koha item type |
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MCK Central Library | MCK Central Library | General Stacks | 616.042 TUR-E16 | 19581 | 12/24/2021 | Books | ||||
MCK Central Library | MCK Central Library | General Stacks | 616.042 TUR-E16 | 19898 | 02/22/2023 | Books |