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Research 31–60 of 402
- 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.
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- 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 with papular lesions: a rare cause of irreversible childhood alopecia
- Congenital atrichia associated with situs inversus and mesocardia
- CONGENITAL ATRICHIA.*
- Congenital atrichia with papular lesions
- Focal atrichia: A diagnostic clue in female pattern hair loss
- Congenital atrichia associated with nevus flammeus: A rare association
- Congenital Atrichia: A Case Report
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Papular atrichia
- 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
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Biology and Genetics of Hair
- Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomized, Placebo-Controlled Phase III Trial
- Inherited ichthyosis: Syndromic forms
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Hair physiology and its disorders
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Genetics of Structural Hair Disorders
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Disease causing homozygous variants in the human hairless gene
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A Case of IFAP Syndrome with Severe Atopic Dermatitis