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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Certain VDR gene changes can affect melanoma risk.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

New genetic variants linked to albinism were found in Pakistani families.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A specific gene mutation causes a severe skin disorder in a family.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

A genetic hair protein variant is more common in Japanese people and is inherited.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

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

A genetic marker linked to a type of hair loss was found in most patients studied.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

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

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

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Genetic differences may influence male pattern hair loss in Russians.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Hair loss gene linked to prostate issues.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

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

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.