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- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Two females with hair loss
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Inherited Disorders of the Hair
- Biology and Genetics of Hair
- Molecular Genetics of Alopecias
- Disease causing homozygous variants in the human hairless gene
- Hair loss and its management in children
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