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Research 30 of 578
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Woolly hair nevus
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- The twisting tale of woolly hair: a trait with many causes
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- A rare case of woolly hair with unusual associations
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Hair Follicle Miniaturization in a Woolly Hair Nevus
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Woolly hair with alopecia areata in a Caucasian girl
- [Wooly hair syndrome. Clinical and microscopic study].
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Woolly hair generalizado: caso clínico e revisão da literatura
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Woolly Hair in Two Siblings
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- WOOLY HAIR PALMOPLANTAR KERATODERMA : A CASE REPORT