enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. X-linked recessive inheritance - Wikipedia

    en.wikipedia.org/wiki/X-linked_recessive_inheritance

    A popular example showing this pattern of inheritance is that of the descendants of Queen Victoria and the blood disease hemophilia. [3] The last pattern seen is that X-linked recessive traits tend to skip generations, meaning that an affected grandfather will not have an affected son, but could have an affected grandson through his daughter. [4]

  3. Sex linkage - Wikipedia

    en.wikipedia.org/wiki/Sex_linkage

    Sex-influenced or sex-conditioned traits are phenotypes affected by whether they appear in a male or female body. [6] Even in a homozygous dominant or recessive female the condition may not be expressed fully. Example: baldness in humans.

  4. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Autosomal recessive inheritance, a 25% chance. Autosomal recessive traits is one pattern of inheritance for a trait, disease, or disorder to be passed on through families. For a recessive trait or disease to be displayed two copies of the trait or disorder needs to be presented. The trait or gene will be located on a non-sex chromosome.

  5. Heredity - Wikipedia

    en.wikipedia.org/wiki/Heredity

    Heredity of phenotypic traits: a father and son with prominent ears and crowns. DNA structure. Bases are in the centre, surrounded by phosphate–sugar chains in a double helix. In humans, eye color is an example of an inherited characteristic: an individual might inherit the "brown-eye trait" from one of the parents. [1]

  6. 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]

  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. Non-Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Non-Mendelian_inheritance

    Individuals can develop a recessive trait in the phenotype dependent on their sex—for example, colour blindness and haemophilia (see gonosomal inheritances). [ 7 ] [ 8 ] As many of the alleles are dominant or recessive, a true understanding of the principles of Mendelian inheritance is an important requirement to also understand the more ...

  9. Hereditary carrier - Wikipedia

    en.wikipedia.org/wiki/Hereditary_carrier

    The individual has both a genetic predisposition for the dominant trait and a genetic predisposition for the recessive trait, and the dominant expression prevails in the phenotype. In an individual which is heterozygous regarding a certain allele, it is not externally recognisable that it also has the recessive allele.