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Research 991–1000 of 1000+
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Genetically separable determinants of hair keratin gene expression
- Keratin expression by corneal and limbal stem cells during development
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- A new type of pachyonychia congenita.