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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

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

The ACE1 gene variant doesn't affect long-COVID symptoms.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Two genetic variations in Moa buffalo help them adapt to heat.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

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New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.