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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

The study found genetic variations in sheep that affect traits like milk production, growth, and health.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Certain genes in European Merino sheep help them adapt to different climates.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Targeting the TNFRSF1B gene may help treat hair loss.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Increasing SSAT makes skin more prone to cancer.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.