enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    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.

  3. Red hair - Wikipedia

    en.wikipedia.org/wiki/Red_hair

    Red hair, also known as ginger hair, is a human hair color found in 2–6% of people of Northern or Northwestern European ancestry and lesser frequency in other populations. It is most common in individuals homozygous for a recessive allele on chromosome 16 that produces an altered version of the MC1R protein. [ 1 ]

  4. Woolly hair - Wikipedia

    en.wikipedia.org/wiki/Woolly_hair

    Woolly hair. Woolly hair is a difficult to brush hair, usually present since birth and typically most severe in childhood. [1] It has extreme curls and kinks, occurs in black people and is distinct from afro-textured hair. [3] The hairs come together to form tight locks, unlike in afro-textured hair, where the hairs remain individual. [1]

  5. Human hair color - Wikipedia

    en.wikipedia.org/wiki/Human_hair_color

    A variety of human hair colors; from top left, clockwise: black, brown, blonde, white, red. Human hair color is the pigmentation of human hair follicles and shafts due to two types of melanin: eumelanin and pheomelanin. Generally, the more melanin present, the darker the hair. Its tone depends on the ratio of black or brown eumelanin to yellow ...

  6. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Mendelian traits in humans. 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. Race and genetics - Wikipedia

    en.wikipedia.org/wiki/Race_and_genetics

    ISBN 978-0-309-70065-8. PMID 36989389. In humans, race is a socially constructed designation, a misleading and harmful surrogate for population genetic differences, and has a long history of being incorrectly identified as the major genetic reason for phenotypic differences between groups.

  8. Simple Mendelian genetics in humans - Wikipedia

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

    OMIM (Online Mendelian Inheritance in Man) [3] is a comprehensive database of human genotype–phenotype links. Many visible human traits that exhibit high heritability were included in the older McKusick's Mendelian Inheritance in Man. Before the discovery of genotyping, they were used as genetic markers in medicolegal practice, including in ...

  9. Rex mutation - Wikipedia

    en.wikipedia.org/wiki/Rex_mutation

    A rex rabbit. The rex mutation is a genetic variation in mammals that results in soft curly fur. These effects are due to changes in the structure of groups of hairs and cross-section of individual hairs. The rexed coats are unusual but occur (and have been preserved) in cats, rats, rabbits, horses, and dogs.