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Research 61–90 of 1000+
- Two females with hair loss
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Keratosis follicularis spinulosa decalvans in a female
- Monilethrix in three generations
- Dermoscopic Features of Pili Annulati: Features of PA
- Marie-unna hereditary hypotrichosis
- Woolly hair generalizado: caso clínico e revisão da literatura
- Pearly Pinna Papules in a Young Female
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Monilethrix – Case report of a rare disease
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Substance P in keratosis follicularis spinulosa decalvans
- Nonscarring hair loss disorders
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia