Results 311 to 320 of about 2,431,050 (332)
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Current Opinion in Pediatrics, 1994
Recent advances in molecular genetics have led to major breakthroughs in the understanding of two heterogeneous groups of inherited skin diseases, epidermolysis bullosa and the ichthyoses. Mutations in keratins K5 or K14 are found in epidermolysis bullosa simplex.
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Recent advances in molecular genetics have led to major breakthroughs in the understanding of two heterogeneous groups of inherited skin diseases, epidermolysis bullosa and the ichthyoses. Mutations in keratins K5 or K14 are found in epidermolysis bullosa simplex.
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Genetics of Alzheimer’s disease
Essays in Biochemistry, 1998Mutations in any one of three genes can cause autosomal dominant, early-onset Alzheimer's disease: these genes are the amyloid precursor protein (APP) gene on chromosome 21, the presenilin-1 (PS-1) gene on chromosome 14 and the presenilin-2 (PS-2) gene on chromosome 1.
M, Hutton, J, Pérez-Tur, J, Hardy
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Distinguishing genetic disease and genetic susceptibility
American Journal of Medical Genetics, 1994AbstractWith the increasing awareness of the involvement of genetic factors in disease, questions arise as to what distinguishes genetic from non‐genetic disease, and what constitutes a genetic susceptibility. A general framework, reflecting the structure of biological explanations, is presented in which such distinctions can be made.
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Current Opinion in Genetics & Development, 2008
Nick, Hastie, Aravinda, Chakravarti
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Nick, Hastie, Aravinda, Chakravarti
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Genetics of disease Complex genetics, complex diseases
Current Opinion in Genetics & Development, 1998, Willard, , Davies
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