Emery's elements of medical genetics (Record no. 129463)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01624nam a22002057a 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20190510124620.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 190510b ||||| |||| 00| 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9780702066856 |
| 082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER | |
| Classification number | QZ50 |
| Item number | EME |
| 100 ## - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Turnpenny, Peter D. |
| 9 (RLIN) | 266 |
| 245 ## - TITLE STATEMENT | |
| Title | Emery's elements of medical genetics |
| 250 ## - EDITION STATEMENT | |
| Edition statement | 15th ed. |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Place of publication, distribution, etc. | Philadelphia: |
| Name of publisher, distributor, etc. | Elsevier, |
| Date of publication, distribution, etc. | 2017 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | x, 400 p.: |
| Dimensions | 26 cm. |
| 500 ## - GENERAL NOTE | |
| General note | Contents:<br/><br/>The history and impact of genetics in medicine<br/><br/>Section A: The scientific basis of human genetics<br/>The cellular and molecular basis of inheritance<br/>Chromosomes and cell division<br/>Finding the cause of monogenic disorders by identifying disease genes<br/>Laboratory techniques for diagnosis of monogenic disorders<br/>Patterns of inheritance<br/>Population and mathematical genetics<br/>Risk calculation<br/><br/>Developmental genetics<br/><br/>Section B: Genetics in medicine and genomic medicine<br/>Common disease, polygenic and multifactorial genetics<br/>Screening for genetic disease<br/>Hemoglobin and the hemoglobinopathies<br/>Immunogenetics<br/>The genetics of cancer and cancer genetics<br/><br/><br/><br/>Pharmacogenetics, personalized medicine and the treatment of genetic disease<br/><br/>Section C: Clinical genetics, counseling, and ethics<br/>Congenital, abnormalities, dysmorphic syndromes, and learning disability<br/>Chromosome disorders<br/>Inborn errors of metabolism<br/>Mainstream monogenetic disorders<br/>Prenatal testing and reproductive genetics<br/>Genetic counseling<br/>Ethical and legal issues in medical genetics. |
| 650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Medical Genetics |
| 9 (RLIN) | 267 |
| 650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name as entry element | Genetics, Medical |
| 9 (RLIN) | 268 |
| 700 ## - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Ellard, Sian |
| 9 (RLIN) | 269 |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Koha item type | Books |
| Withdrawn status | Lost status | Source of classification or shelving scheme | Damaged status | Not for loan | Home library | Current library | Shelving location | Date acquired | Total Checkouts | Total Renewals | Full call number | Barcode | Date last seen | Date last checked out | Price effective from | Koha item type |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Library and Information Centre | Library and Information Centre | Book section | 10/05/2019 | 5 | 6 | QZ50 EME | 29961 | 01/03/2022 | 24/12/2021 | 10/05/2019 | Books |