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Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Hair loss gene found on chromosome 3q26.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A mutation in mice causes hair loss and immune problems.

A gene mutation in mice causes permanent hair loss and skin issues.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

New genes linked to male pattern baldness were found on chromosome 20p11.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The scraggly mutation causes hair loss and skin defects in mice.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Chromosomal differences affect how muscle cells respond to testosterone.

A patient with a rare chromosome condition also had a rare type of hair loss.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Scientists found a gene in mice that causes early hearing loss.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Two mouse mutations cause similar hair loss despite different skin changes.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.