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Research 991–1000 of 996
- A missense mutation in Lama3 causes androgen alopecia
- Developmental Mapping of Hair Follicles in the Embryonic Stages of Cashmere Goats Using Proteomic and Metabolomic Construction
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Pathogenesis of androgenetic alopecia
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Clouston’s syndrome: a rare case report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide