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- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- 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 novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Molecular basis of congenital atrichia in humans and mice.
- Congenital atrichia and hypotrichosis
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Congenital atrichia with papular lesions
- Congenital atrichia associated with situs inversus and mesocardia
- CONGENITAL ATRICHIA.*
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Congenital atrichia with papular lesions
- Congenital atrichia associated with nevus flammeus: A rare association
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Congenital Atrichia: A Case Report
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Papular atrichia
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Hair Loss in Children
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Clinical and molecular genetic studies in hereditary hair loss
- Facial Hair Transplantation