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- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- PA31 Congenital alopecia areata: a systematic review
- Congenital alopecia areata
- Cutaneous Mastocytosis Associated With Congenital Alopecia
- Congenital triangular alopecia: A close mimicker of alopecia areata
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Congenital Combined Melanocytic Nevus of the Scalp With Associated Alopecia Areata
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