Thompson & Thompson genetics in medicine / 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 Ressearch 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.
Publisher: Philadelphia : Elsevier, [2016]Copyright date: ©2016Edition: Eighth editionDescription: xi, 546 pages : illustrations ; 28 cmContent type: text Media type: unmediated Carrier type: volumeISBN: 9781437706963 (alk. paper); 1437706967 (alk. paper)Other title: Genetics in medicine | Thompson and Thompson genetics in medicineSubject(s): Medical genetics | Genetics, MedicalItem type | Current location | Call number | Status | Date due | Barcode |
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Reserve Books | St Luke's College of Medicine Library Reserve Section | RB 155 .N86 2016 (Browse shelf) | Available | 005620 |
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RB 145 T87 2012 Clinical hematology : | RB 155 A35 2012 Elsevier's integrated review genetics / | RB 155 G86 2011 Essentials of medical genetics for health professionals / | RB 155 .N86 2016 Thompson & Thompson genetics in medicine / | RB 155 S33 2014 Medical genetics : | RC 37 .B63 2009 BOC study guide: clinical laboratory: certification examinations/ | RC 46 A53 2010 Andreoli and Carpenter's Cecil essentials of medicine / |
Originally published under the title: Genetics in medicine / James S. Thompson and Margaret W. Thompson.
Includes bibliographical references and index.
Introduction 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.
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