000 | 03098nam a22003497a 4500 | ||
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003 | ZW-GwMSU | ||
005 | 20240509130543.0 | ||
008 | 240430b |||||||| |||| 00| 0 eng d | ||
020 | _a9781437706963 (alk. paper) | ||
020 | _a1437706967 (alk. paper) | ||
040 |
_arda _cMSULIB _erda _bEnglish |
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050 | 0 | 0 | _aRB155 NUS |
100 | 1 |
_aNussbaum, Robert L., _d1950- , _eauthor. |
|
245 | 1 | 0 |
_aThompson & Thompson genetics in medicine / _ccreated by Robert L. Nussbaum,MD, FACP, FACMG, Holly Smith Chair of Medicine and Science, Professor of Medicine, Neurology, Pediatrics and Pathology, Department of Medicine and Institute for Human Genetics, University of California San Francisco, San Francisco, California, Roderick R. McInnes, CM, MD, PhD, FRS(C), FCAHS, FCCMG, Alva Chair in Human Genetics, Canada Research Chair in Neurogenetics, Professor of Human Genetics and Biochemistry, Director, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada, Huntington F. Willard, PhD, President and Director, The Marine Biological Laboratory, Woods Hole, Massachusetts, and Professor of Human Genetics, University of Chicago, Chicago, Illinois ; with clinical cases updated by Ada Hamosh, MD, MPH, Professor of Pediatrics, McKusick-Nathans Institute of Genetic Medicine, Scientific Director, OMIM, Johns Hopkins University School of Medicine, Baltimore, Maryland. |
246 | 1 | _aGenetics in medicine | |
246 | 1 | _aThompson and Thompson genetics in medicine | |
250 | _aEighth edition. | ||
264 | 1 |
_bElsevier, _c[2016] |
|
264 | 4 | _c©2016 | |
300 |
_axi, 546 pages : _billustrations ; _c28 cm |
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336 |
_atext _2rdacontent |
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337 |
_aunmediated _2rdamedia _bn |
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338 |
_avolume _2rdacarrier _bnc |
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500 | _aOriginally published under the title: Genetics in medicine / James S. Thompson and Margaret W. Thompson. | ||
504 | _aIncludes bibliographical references and index. | ||
505 | 0 | _aIntroduction to the human genome -- The human genome: gene structure and function -- Human genetic diversity: mutation and polymorphism -- Principles of clinical cytogenetics and genome analysis -- The chromosomal and genomic basis of disease: disorders of the autosomes and sex chromosomes -- Patterns of single-gene inheritance -- Complex inheritance of common multifactorial disorders -- Genetic variation in populations -- Identifying the genetic basis for human disease -- The molecular basis of genetic disease : general principles and lessons from the hemoglobinopathies -- The molecular, biochemical, and cellular basis of genetic disease -- The treatment of genetic disease -- Developmental genetics and birth defects -- Cancer genetics and genomics -- Risk assessment and genetic counseling -- Prenatal diagnosis and screening -- Application of genomics to medicine and personalized health care -- Ethical and social issues in genetics and genomics. | |
650 | 0 | _aMedical genetics. | |
650 | 1 | 2 | _aGenetics, Medical. |
700 | 1 |
_aMcInnes, Roderick R., _eauthor. |
|
700 | 1 |
_aWillard, Huntington F., _eauthor. |
|
942 |
_2lcc _cB |
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999 |
_c165241 _d165241 |