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  2. Human hair color - Wikipedia

    en.wikipedia.org/wiki/Human_hair_color

    The Fischer–Saller scale, named after Eugen Fischer and Karl Saller is used in physical anthropology and medicine to determine the shades of hair color. The scale uses the following designations: A (very light blond), B to E (light blond), F to L (), M to O (dark blond), P to T (light brown to brown), U to Y (dark brown to black) and Roman numerals I to IV and V to VI (red-blond).

  3. Fischer–Saller scale - Wikipedia

    en.wikipedia.org/wiki/Fischer–Saller_scale

    The Fischer–Saller Scale, named for eugenicist Eugen Fischer and German anthropologist Karl Saller , is used in physical anthropology and medicine to determine the shades of hair color. The scale uses the following designations: [1] [2] [3] [4]

  4. Pattern hair loss - Wikipedia

    en.wikipedia.org/wiki/Pattern_hair_loss

    Pattern hair loss (also known as androgenetic alopecia (AGA) [1]) is a hair loss condition that primarily affects the top and front of the scalp. [2] [3] In male-pattern hair loss (MPHL), the hair loss typically presents itself as either a receding front hairline, loss of hair on the crown and vertex of the scalp, or a combination of both.

  5. Why your hair and eye colors change

    www.aol.com/news/2014-07-23-why-your-hair-and...

    Melanin is the protein that creates skin, eye and hair color. More melanin means darker eyes, hair or skin. The color of the melanin in the eyes is determined by three other genes, EYCL1, 2 and 3.

  6. Millions Of People Take Biotin For Hair Growth, And Many Are ...

    www.aol.com/millions-people-biotin-hair-growth...

    Changes in hair: You may start to notice thinning, hair loss, brittleness, or dryness. Changes in skin : This often looks like noticeable dryness, flaky, or scaly skin, especially around the eyes ...

  7. 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.

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