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- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
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- Congenital atrichia with papular lesions
- FOXN1 deficient nude severe combined immunodeficiency
- Congenital atrichia with papular lesions
- Alopezien und Hypotrichosen im Kindesalter
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Atrichia with papular lesions
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Congenital Atrichia: A Case Report
- Biology and Genetics of Hair
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- An Update of Congenital Adrenal Hyperplasia
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Alopecia totalis in an infant
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Alopecia: Association with Resistance to Thyroid Hormones
- Alopecia areata in a rhesus monkey (Macaca mulatta)
- Congenital atrichia and hypotrichosis
- Alopecia in Epidermolysis Bullosa
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Inherited Disorders of the Hair