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- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Woolly Hair in Two Siblings
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Monilethrix
- Congenital and Hereditary Skin Diseases
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
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