eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

Browse by Topic

  1. Biochemistry
  2. Bioethics & Philosophy
  3. Cell Biology
  4. Developmental Biology
  5. Ecology
  6. Evolution & Diversity of Life
  7. Genetics & Disease
    1. Bioinformatics and Genetic Disease
    2. Cancer Genetics
    3. Chromosomal Disorders
    4. Epigenetics and Disease
    5. Forensic Genetics
    6. Gene and Genome Structure and Organisation
    7. Gene Expression Profiling of Genetic Disease
    8. Gene Mapping by Disease Association
    9. Gene Therapy
    10. General Genetics and Disease
    11. Genetic Counseling
    12. Genetic Models
    13. Genetics of Intelligence and Cognition
    14. Genomic Disorders
    15. Inter-Individual Variation and Polymorphism
    16. Linkage Analysis
      1. Absolute Pitch: Genetics
      2. Alcoholism: Collaborative Study on the Genetics of Alcoholism (COGA)
      3. Alzheimer Disease, Genetics of
      4. Analysis of Gene–Gene Interactions Underlying Human Disease
      5. Bardet-Biedl Syndrome, an Oligogenic Disease
      6. Behaviour Genetics – Human
      7. Beyond the Genome
      8. Bioethics: ELSI
      9. You have free access to this content
        Bioinformatics
      10. Biological/Biochemical Features and Molecular Genetics of Specific Language Impairment (SLI)
      11. Brain Cancers
      12. Chimera-directed Gene Repair
      13. Colon Cancer
      14. deCODE: A Genealogical Approach to Human Genetics in Iceland
      15. Disease-related Genes: Identification
      16. Dopamine D4 Receptor (DRD4) Box Score
      17. Epidemiological Tools
      18. Facioscapulohumeral Muscular Dystrophy: Genetics
      19. Gene Feature Identification
      20. Gene Mapping: Comparative
      21. Genetic Determinants of Human Life-Span
      22. Genetic Distance and Mapping Functions
      23. Genetic Epidemiology of Smoking Behaviour and Nicotine Dependence
      24. Genetic Isolates and Behavioral Gene Searches
      25. Genetic Linkage Mapping
      26. Genetic Networks
      27. Genetic Susceptibility to Autoimmune Disorders
      28. Genetics of Athletic Performance
      29. Genetics of Depression
      30. Genetics of Graves' Disease
      31. Genetics of Keratoconus
      32. Genetics of Nicotine Addiction
      33. Genetics of Pheochromocytoma
      34. Genetics of Preterm Birth
      35. Genetics of Susceptibility to Tuberculosis
      36. Genome Mapping
      37. Genome-wide Association Studies
      38. Genome-wide Association Studies: The Success, Failure and Future
      39. Gibbs Sampling and Bayesian Inference
      40. Haplotype Sharing Methods
      41. High-Throughput Single Nucleotide Polymorphisms Genotyping Technologies
      42. History of Classical Genetics
      43. Human Genetics: Online Resources
      44. Hypertrophic Cardiomyopathy
      45. Identification of Disease Genes by CGH Microarrays
      46. Identifying Genes Underlying Human Inherited Disease
      47. Infectomics: Study of Microbial Infections Using Omic Approaches
      48. Inflammatory Bowel Disease, Genetics of
      49. Insulin-dependent Diabetes Mellitus (IDDM): Identifying the Disease-causing Gene at the IDDM11 Locus
      50. Leukaemias and Lymphomas
      51. Linkage Analysis
      52. Linkage Analysis Software
      53. Linkage and Association Studies
      54. Linkage and Association Studies: Replication
      55. Linkage and Crossing over
      56. Lod Score
      57. Markov Chain Monte Carlo Methods
      58. Melanoma
      59. Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping
      60. Microarrays: Use in Mutation Detection
      61. Migraine: Genetics
      62. Model-based Linkage Analysis
      63. Modifier Genes in the Haemoglobinopathies
      64. Molecular Genetic Analysis of Ménière's Disease
      65. Molecular Genetics of Anxiety
      66. Molecular Genetics of Bipolar Disorder
      67. Molecular Genetics of Cardiac Arrhythmias
      68. Molecular Genetics of Cardiovascular Disease
      69. Molecular Genetics of Chronic Obstructive Pulmonary Disease
      70. Molecular Genetics of Coeliac Disease
      71. Molecular Genetics of Crohn Disease
      72. Molecular Genetics of Emery–Dreifuss Muscular Dystrophy
      73. Molecular Genetics of Endometriosis
      74. Molecular Genetics of Hereditary Spastic Paraplegias
      75. Molecular Genetics of Hereditary Spastic Paraplegias
      76. Molecular Genetics of Ischaemic Stroke
      77. Molecular Genetics of Myocardial Infarction
      78. Molecular Genetics of Parkinsonism
      79. Molecular Genetics of Susceptibility to Coronary Heart Disease
      80. Molecular Genetics of Tourette Syndrome
      81. Molecular Genetics of Type 1 Diabetes
      82. The Molecular Genetics of Type 2 Diabetes: Past, Present and Future
      83. Mood Disorders: Molecular
      84. Mouse N-ethyl-N-nitrosourea (ENU) Mutagenesis
      85. Multilocus Linkage Analysis
      86. Multiple Significance Testing in Genetic Epidemiology
      87. Multiple Testing in Genetic Epidemiology
      88. Parametric and Nonparametric Linkage Analysis
      89. Path Analysis in Genetic Epidemiology
      90. Population History and Linkage Disequilibrium
      91. Population Stratification, Adjustment for
      92. Porphyrias: Genetics
      93. Prostate Cancer
      94. Prostate Cancer
      95. Psychoses
      96. Relatives-based Nonparametric Analysis of Linkage
      97. Relatives-based Test for Linkage Disequilibrium: The Transmission/Disequilibrium Test (TDT)
      98. Research on Rare Variants for Complex Diseases
      99. Restriction Fragment Length Polymorphism (RFLP)
      100. Role of Polymorphisms in Cancer Susceptibility
      101. Sample Size Requirements
      102. Schizophrenia and Bipolar Disorder: Linkage on Chromosomes 5 and 11
      103. Schizophrenia: Molecular Genetics
      104. Segregation Analysis Software
      105. Sexual Orientation
      106. Susceptibility Genes: Detection
      107. Systemic Lupus Erythematosus: Genetic and Epigenetic View
      108. Systems Biology: Genomics Aspects
      109. The Genetics of Stuttering
      110. Tuberous Sclerosis Complex and the Mammalian Target of Rapamycin Pathways
      111. Whole Genome Resequencing and 1000 Genomes Project
    17. Mitochondrial Diseases
    18. Model Organisms and Human Disease
    19. Molecular Genetics of Common and Complex Disease
    20. Mutational Mechanisms of Genetic Disease
    21. Pharmacogenetics and Pharmacogenomics
    22. Proteomic Studies of Genetic Disease
    23. Quantitative Genetics
    24. Specific Genetic Disorders
    25. Statistical Methodology in Genetics
    26. Techniques and Tools in Clinical Genetics
  8. Immunology
  9. Microbiology
  10. Molecular Biology
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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