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The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Haplogroup X found in Altaian population supports Amerindian origin.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Farudodstat may effectively treat alopecia areata without harmful side effects.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Certain genetic variations are linked to hair loss in Mexican men.

New genetic mutations causing hair loss were found in a Chinese family.

A specific gene mutation causes sparse, brittle hair in a family.

Certain gene variations may increase the risk of hair loss in Egyptians.

CCL5 is important for the hair growth potential of human dermal papilla cells.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

AGD1's PH domain is essential for its role in root hair growth and polarity.

A gene mutation in Lama3 is linked to a common type of hair loss.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

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.

The hr gene is linked to hair loss in Valle del Belice sheep.

DNMT3A is crucial for healthy skin and hair growth.

Mutations in the hairless gene cause a rare form of permanent hair loss.