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  2. Simple Mendelian genetics in humans - Wikipedia

    en.wikipedia.org/wiki/Simple_Mendelian_genetics...

    Mendelian traits behave according to the model of monogenic or simple gene inheritance in which one gene corresponds to one trait. Discrete traits (as opposed to continuously varying traits such as height) with simple Mendelian inheritance patterns are relatively rare in nature, and many of the clearest examples in humans cause disorders.

  3. 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 .

  4. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]

  5. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    Mendelian inheritance (also known as Mendelism) is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson. [1] These principles were initially controversial.

  6. Thomas Hunt Morgan bibliography - Wikipedia

    en.wikipedia.org/wiki/Thomas_Hunt_Morgan...

    This is a list of books and monographs by the American geneticist Thomas Hunt Morgan. Morgan produced 22 books on embryology, genetics and evolution. Books are in order by date. Three of Morgan's co-authors have their own articles: Calvin Bridges, Alfred Sturtevant and Hermann Joseph Muller.

  7. Human genetic variation - Wikipedia

    en.wikipedia.org/wiki/Human_genetic_variation

    The study of human genetic variation has evolutionary significance and medical applications. It can help scientists reconstruct and understand patterns of past human migration. In medicine, study of human genetic variation may be important because some disease-causing alleles occur more often in certain population groups.

  8. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    This is an accepted version of this page This is the latest accepted revision, reviewed on 11 January 2025. 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 ...

  9. 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 sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.