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- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Atrichia with papular lesions
- Congenital atrichia with papular lesions
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Morphological Approach to Hair Disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Male fertility and skin diseases
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Alopecia and Thyroid Disease
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- 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.
- Genetic Hair Disorders: A Review
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Oral Presentations
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes