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Research 61–90 of 1000+
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Alopezien und Hypotrichosen im Kindesalter
- Woolly Antics between the Sheaths
- Woolly hair generalizado: caso clínico e revisão da literatura
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
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- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Research Snippets
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Current Genetics in Hair Diseases
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants