Medical Genetics

Medical Genetics
ISBN-10
032303568X
ISBN-13
9780323035682
Series
Medical Genetics
Category
Genetic disorders
Pages
363
Language
English
Published
2003
Publisher
Mosby Incorporated
Authors
Lynn B. Jorde, John C. Carey, Michael J. Bamshad

Description

This is one of the few medical genetics texts on a 2-year revision cycle. It provides up-to-date information that can be read, retained, and applied with ease! The 3rd Edition covers pharmacogenomics, the societal implications of technologies, the Human Genome Project, cloning, genetic enhancement, and embryonic stem cell research, new tumor suppressor genes and oncogenes, and more. Mini-summaries, study questions, suggested readings, and a detailed glossary facilitate review of the material. Clinical relevance is demonstrated in over 230 photographs, illustrations, and tables as well as boxes containing patient/family vignettes. Its coverage includes ethical, legal, and social issues and clinical commentary on important genetic diseases. A companion web site offers continuing updates and a wealth of additional features. The smart way to study! Elsevier titles with STUDENT CONSULT will help you master difficult concepts and study more efficiently in print and online! Perform rapid searches. Integrate bonus content from other disciplines. Download text to your handheld device. And a lot more. Each STUDENT CONSULT title comes with full text online, a unique image library, case studies, USMLE style questions, and online note-taking to enhance your learning experience. Your purchase of this book entitles you to access www.studentconsult.com at no extra charge. This innovative web site offers you... Access to the complete text and illustrations of this book. Integration links to bonus content in other STUDENT CONSULT titles. Content clipping for your handheld. An interactive community center with a wealth of additional resources. The more STUDENT CONSULT titles you buy, the more resources you can access online! Look for the STUDENT CONSULT logo on your favorite Elsevier textbooks!

Other editions

Similar books

  • The Metabolic Basis of Inherited Disease
    By Charles R. Scriver, John Bruton Stanbury

    OKA M , KATABUCHI H , MUNEMURA M , MIZUMOTO J , MAEYAMA M : An unusual case of male pseudohermaphroditism ... JACOBS PA , BAIKIE AG , COURT BROWN WM , FORREST H , ROY JR , STEARD JSS , LENNOX B : Chromosomal sex in the syndrome of ...

  • Beauty: A Novel
    By Susan Wilson

    For centuries the Cromptons have had their portraits painted by the Millers. But when Alix Miller accepts a commision from Lee Crompton to paint his portrait, she little suspects that it will change her life.

  • Structure-function Relationship of K+ Ion Channel Toxins: From Cloning to Functional Characterization
    By Isabelle Huys

    Tempel , B. L. , Y. N. Jan , and L. Y. Jan. 1988. Cloning of a probable potassium channel gene from mouse brain . Nature . 332 : 837-9 . Tenenholz , T. C. , R. S. Rogowski , J. H. Collins , M. P. Blaustein , and D. J. Weber . 1997 .

  • Syndromes of the Head and Neck
    By Robert J. Gorlin

    1. Deformations and Disruptions2. Teratogenic Agents3. Chromosomal Syndromes: Common and/or Well-Known Syndromes4. Chromosomal Syndromes: Unusual Variants5. Metabolic Disorders6. Syndromes Affecting Bone: The Osteogenesis Imperfectas7. Syndromes Affecting Bone: Chondrodysplasias and Chondrodystrophies8....

  • Emery and Rimoin's Principles and Practice of Medical Genetics
    By Alan E. H. Emery, David L. Rimoin

    Emery and Rimoin's Principles and Practice of Medical Genetics

  • Brave New NHS?: The Impact of the New Genetics on the Health Service
    By Jo Lenaghan

    Genetic testing and screening Current guidelines for genetic testing Suggested criteria for the introduction of genetic tests Current guidelines for genetic screening Criteria for genetic screening Review of current decision - making ...

  • Alagille Syndrome: Pathogenesis and Clinical Management
    By Binita M. Kamath, Kathleen M. Loomes

    The book reviews the pathophysiology and genetics of the disorder, discusses recent molecular advances and its impact on diagnostics, and describes management challenges and strategies. The text also touches upon future treatment options.

  • Missing Genetic Pieces: Strategies for Living with VCFS, the Chromosome 22q11 Deletion
    By Sherry Baker-Gomez

    VCFS is also referred to as Velo Cardio Facial Syndrome, CHARGE Syndrome, Shprintzen Syndrome, DiGeorge Sequence, Pierre Robin Sequence, Potter Sequence.

  • Rethinking IT and Health
    By Jo Lenaghan

    PC based multimedia systems , usually stored on CD - ROM , are combining text , sound , pictures , video clips etc. in an ... Medical Decision Making ( Kasper et al Empowering the patient and public through information technology 131.

  • The Metabolic & Molecular Bases of Inherited Disease
    By Charles R. Scriver

    Presents clinical, biochemical, and genetic information concerning those metabolic anomalies grouped under inborn errors of metabolism.