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Research 31–60 of 1000+
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Woolly Hair in Two Siblings
- Woolly hair generalizado: caso clínico e revisão da literatura
- Biology and Genetics of Hair
- Molecular Basis of Hereditary Hair Diseases
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Current Genetics in Hair Diseases
- Woolly Antics between the Sheaths
- Enanthem in Patients With COVID-19 and Skin Rash
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Inherited Disorders of the Hair
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Alopezien und Hypotrichosen im Kindesalter
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Woolly hair nevus
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope