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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
- Hair biology and hair loss disorders: An update and new concepts
- Hair loss disorders in domestic animals
- Methods of hair loss evaluation in patients with endocrine disorders.
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Hair and nail disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Hair Loss in Children
- AN UPDATE OF HAIR SHAFT DISORDERS
- Hair loss.
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Clinical and molecular genetic studies in hereditary hair loss
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hair Disorders
- Clinical relevance of hair microscopy in alopecia
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Congenital and Hereditary Skin Diseases
- Eyelashes: Anatomical and Physiological Features, Eyelash Loss and Trichomegaly: Review
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Hairless: A nuclear receptor corepressor essential for skin function
- Hairless is a nuclear receptor corepressor essential for skin function
- The eye and the skin in endocrine metabolic diseases
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Alopecia in children
- Alopecia areata - probing the deforestation
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis