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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. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    An example of the codominant inheritance of some of the four blood groups. Mendelian traits in humans are human traits that are substantially influenced by Mendelian inheritance . Most – if not all – Mendelian traits are also influenced by other genes, the environment, immune responses, and chance.

  4. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    When the tall allele was present, the plant would be tall, even if the plant was heterozygous. In order for the plant to be short, it had to be homozygous for the recessive allele. [8] [9] One way this can be illustrated is using a Punnett square. In a Punnett square, the genotypes of the parents are placed on the outside. An uppercase letter ...

  5. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    Characteristics Mendel used in his experiments [24] P-Generation and F 1-Generation: The dominant allele for purple-red flower hides the phenotypic effect of the recessive allele for white flowers. F 2-Generation: The recessive trait from the P-Generation phenotypically reappears in the individuals that are homozygous with the recessive genetic ...

  6. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Autosomal recessive inheritance, a 25% chance, and (purple) a 50% carrier 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.

  7. Sex linkage - Wikipedia

    en.wikipedia.org/wiki/Sex_linkage

    Illustration of some X-linked heredity outcomes (A) the affected father has one X-linked dominant allele, the mother is homozygous for the recessive allele: only daughters (all) will be affected. (B) the affected mother is heterozygous with one copy of the X-linked dominant allele: both daughters and sons will have 50% probability to be ...

  8. Classical genetics - Wikipedia

    en.wikipedia.org/wiki/Classical_genetics

    The phenotype is a general term that defines an individual's visible, physical traits. The genotype of an offspring is known as its genetic makeup. The alleles of genes can either be dominant or recessive. A dominant allele needs only one copy to be expressed while a recessive allele needs two copies (homozygous) in a diploid organism to be ...

  9. Inbreeding - Wikipedia

    en.wikipedia.org/wiki/Inbreeding

    Inbreeding is also used to reveal deleterious recessive alleles, which can then be eliminated through assortative breeding or through culling. In plant breeding, inbred lines are used as stocks for the creation of hybrid lines to make use of the effects of heterosis. Inbreeding in plants also occurs naturally in the form of self-pollination.