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  2. Heredity - Wikipedia

    en.wikipedia.org/wiki/Heredity

    Heredity, also called inheritance or biological inheritance, is the passing on of traits from parents to their offspring; either through asexual reproduction or ...

  3. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    This is an accepted version of this page This is the latest accepted revision, reviewed on 10 December 2024. Science of genes, heredity, and variation in living organisms This article is about the general scientific term. For the scientific journal, see Genetics (journal). For a more accessible and less technical introduction to this topic, see Introduction to genetics. For the Meghan Trainor ...

  4. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Human genetics is the study of inheritance as it occurs in human beings.Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.

  5. Genotype–phenotype distinction - Wikipedia

    en.wikipedia.org/wiki/Genotype–phenotype...

    T 1 represents the genetic and epigenetic laws, the aspects of functional biology, or development, that transform a genotype into phenotype. This is the " genotype–phenotype map ". T 2 is the transformation due to natural selection, T 3 are epigenetic relations that predict genotypes based on the selected phenotypes and finally T 4 the rules ...

  6. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    Conversely, some phenotypes could be the result of multiple genotypes. The genotype is commonly mixed up with the phenotype which describes the result of both the genetic and the environmental factors giving the observed expression (e.g. blue eyes, hair color, or various hereditary diseases).

  7. Introduction to genetics - Wikipedia

    en.wikipedia.org/wiki/Introduction_to_genetics

    Genetic disorders are diseases that are caused by a single allele of a gene and are inherited in families. These include Huntington's disease , cystic fibrosis or Duchenne muscular dystrophy . Cystic fibrosis, for example, is caused by mutations in a single gene called CFTR and is inherited as a recessive trait.

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  9. Genetic variation - Wikipedia

    en.wikipedia.org/wiki/Genetic_variation

    Genetic variation can be identified at many levels. Identifying genetic variation is possible from observations of phenotypic variation in either quantitative traits (traits that vary continuously and are coded for by many genes, e.g., leg length in dogs) or discrete traits (traits that fall into discrete categories and are coded for by one or a few genes, e.g., white, pink, or red petal color ...