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- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital hair loss disorders: Rare, but not too rare
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- An Approach to Hair Loss in Pediatric Primary Care
- Diagnosis and Management of Hair Loss in Pediatric
- Hair biology and hair loss disorders: An update and new concepts
- Methods of hair loss evaluation in patients with endocrine disorders.
- Hair loss.
- Hair Loss in Children
- Hair Loss in Children
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hair loss disorders in domestic animals
- Hair loss and its Unani concept and management
- Clinical and molecular genetic studies in hereditary hair loss
- Analysis of hair loss in young adults- A clinical study
- Hair loss: An epidemiologic approach
- 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
- Hair loss in infancy and childhood
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- A Neonate with Unexplained Hair Loss
- Hair loss in infancy and childhood
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Dysfunction of Hair Growth
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Congenital atrichia with papular lesions