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Monilethrix is generally considered to be an autosomal-dominant disorder with variable penetrance. It is caused by mutations of… Expand We analyzed a cohort of 61 follicular lymphomas (FL) with an abnormal G-banded karyotype by spectral karyotyping (SKY) to better… Expand Abstract: Diffuse non‐epidermolytic palmoplantar keratoderma (NEPPK) belongs to the heterogeneous group of skin diseases… Expand Human hHb1 belongs to the type II hard keratin family and is physiologically expressed in hair shafts. In the present study… Expand Monilethrix is characterized by beaded or moniliform hair, which results from the periodic thinning of the hair shaft. The beaded… Expand Epidermolysis bullosa simplex (EBS) is a group of autosomal dominant skin diseases characterized by blistering, due to mechanical… Expand Mapping studies of functional keratin genes in the human genome have localized most of the acidic keratin genes to chromosome… Expand Hereditary palmoplantar keratoderma is characterized by hyperkeratosis of the skin of palms and soles. An autosomal dominant form… Expand Epidermolysis bullosa simplex (EBS) is a group of autosomal dominant skin diseases characterized by blistering, due to mechanical… Expand Epidermolysis bullosa simplex (EBS) is a dominantly inherited genodermatosis characterized by intraepidermal blister formation… Expand