Thompson & Thompson Genetics in Medicine E-Book

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English
941 Pages
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Description

Through six editions, Thompson & Thompson's Genetics in Medicine has been a well-established favorite textbook on this fascinating and rapidly evolving field, integrating the classic principles of human genetics with modern molecular genetics to help you understand a wide range of genetic disorders. The 7th edition incorporates the latest advances in molecular diagnostics, the Human Genome Project, and much more. More than 240 dynamic illustrations and high-quality photos help you grasp complex concepts more easily.

  • This title includes additional digital media when purchased in print format. For this digital book edition, media content is not included.
    • Acquire the state-of-the-art knowledge you need on the latest advances in molecular diagnostics, the Human Genome Project, pharmacogenetics, and bio-informatics.
    • Better understand the relationship between basic genetics and clinical medicine with a variety of clinical case studies.
    • Recognize a wide range of genetic disorders with visual guidance from more than 240 dynamic illustrations and high-quality photos.
    • This title includes additional digital media when purchased in print format. For this digital book edition, media content is not included.

    Subjects

    Books
    Savoirs
    Medicine
    Osteogénesis imperfecta
    Genetta genetta
    Herencia Mendeliana en el Hombre
    Oncogén
    Genoma mitocondrial
    Genetic structure
    Oncology
    Sex chromosome disorders
    Klinefelter's syndrome
    Photocopier
    Alzheimer's disease
    Mental retardation
    Mannan-binding lectin
    Clinical Medicine
    Chromosome abnormality
    Nuchal scan
    Beta-thalassemia
    Greig cephalopolysyndactyly syndrome
    Medical genetics
    Neural tube defect
    Personalized medicine
    Isochromosome
    Medical research
    Pharmacogenetics
    Family medicine
    Human genetics
    Protein S
    Missense mutation
    Neoplasm
    Germline mutation
    Pharmacogenomics
    Duchenne muscular dystrophy
    Children's hospital
    Newborn screening
    Biological agent
    Nonsense mutation
    Chorionic villus sampling
    Homocystinuria
    Anesthetic
    Prenatal diagnosis
    Quantitative trait locus
    Fetal alcohol syndrome
    Satellite DNA
    Hematopoietic stem cell transplantation
    Physician assistant
    Gene duplication
    Public health
    Genetic variation
    Sibling
    Cytogenetics
    Biopsy
    Congenital disorder
    Hirschsprung's disease
    Thalassemia
    Genetic counseling
    Cleft lip and palate
    Severe combined immunodeficiency
    Pseudogene
    Criticism
    Risk assessment
    Major histocompatibility complex
    Oligonucleotide
    Polydactyly
    Karyotype
    Miscarriage
    Medical ultrasonography
    Homology (biology)
    Globin
    Hemoglobinopathy
    Hematology
    Achondroplasia
    Genomics
    Cystic fibrosis
    Philadelphia
    Turner syndrome
    Trisomy
    Tumor suppressor gene
    Tool
    Data storage device
    Pediatrics
    Phenylketonuria
    Nucleic acid
    Messenger RNA
    Mechanics
    Molecule
    Hemoglobin
    Gene therapy
    Genetic disorder
    Genome
    Genetic code
    Eugenics
    Down syndrome
    Complementary DNA
    Biochemistry
    Allele
    Antibacterial
    National Cancer Institute
    Human
    Canada
    Probe
    Gene
    Gari
    Cytochrome P450
    Genetics
    Diane
    Corpus iuris civilis
    Ilex
    Electronic
    SNP
    Mutation
    Intron
    National Institutes of Health
    DNA
    Copyright
    Enzyme

    Informations

    Published by
    Published 01 August 2007
    Reads 0
    EAN13 9781437700930
    Language English
    Document size 12 MB

    Legal information: rental price per page 0.0241€. This information is given for information only in accordance with current legislation.

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