enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 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]

  3. 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]

  4. Particulate inheritance - Wikipedia

    en.wikipedia.org/wiki/Particulate_inheritance

    Gregor Mendel, the Father of Genetics William Bateson Ronald Fisher. Particulate inheritance is a pattern of inheritance discovered by Mendelian genetics theorists, such as William Bateson, Ronald Fisher or Gregor Mendel himself, showing that phenotypic traits can be passed from generation to generation through "discrete particles" known as genes, which can keep their ability to be expressed ...

  5. Sex-determination system - Wikipedia

    en.wikipedia.org/wiki/Sex-determination_system

    In 1866, Gregor Mendel published on inheritance of genetic traits. This is known as Mendelian inheritance and it eventually established the modern understanding of inheritance from two gametes. In 1902, C.E. McClung identified sex chromosomes in bugs. In 1917, C.E. Allen, discovered sex determination mechanisms in plants.

  6. 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 ...

  7. 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 ...

  8. Boveri–Sutton chromosome theory - Wikipedia

    en.wikipedia.org/wiki/Boveri–Sutton_chromosome...

    The Boveri–Sutton chromosome theory (also known as the chromosome theory of inheritance or the Sutton–Boveri theory) is a fundamental unifying theory of genetics which identifies chromosomes as the carriers of genetic material. [1] [2] [3] It correctly explains the mechanism underlying the laws of Mendelian inheritance by identifying ...

  9. Punnett square - Wikipedia

    en.wikipedia.org/wiki/Punnett_square

    The Punnett square is a visual representation of Mendelian inheritance, a fundamental concept in genetics discovered by Gregor Mendel. [10] For multiple traits, using the "forked-line method" is typically much easier than the Punnett square.