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Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

The rs1128977 gene variant may affect cholesterol and body measurements.

Two new gene mutations cause a rare hair disorder.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Certain genetic variants may increase the risk of developing PCOS.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

STK11 gene polymorphism does not predict metformin response in PCOS.

Genetic variations may affect how well finasteride works for BPH patients.

Genetic factors in PCOS are complex, with potential influences from the MC4R gene.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

A certain gene variation can affect protein production and is linked to male pattern baldness.

No significant link was found between the studied genes and female hair loss in the Polish population.

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