Basic defects in Marfan syndrome.
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[1] R. Boucek,et al. The Marfan syndrome: a deficiency in chemically stable collagen cross-links. , 1981, The New England journal of medicine.
[2] S. Faro,et al. Cloning a cDNA for the pro-alpha 2 chain of human type I collagen. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[3] G. Barsh,et al. Altered secretion of type III procollagen in a form of type IV Ehlers-Danlos syndrome. Biochemical studies in cultured fibroblasts. , 1981, Laboratory investigation; a journal of technical methods and pathology.
[4] L. Peltonen,et al. Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VII. , 1980, The Journal of biological chemistry.
[5] D. Botstein,et al. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.
[6] D. Eyre,et al. Collagen: molecular diversity in the body's protein scaffold , 1980, Science.
[7] K. Kivirikko,et al. [Biosynthesis of collagen and its disorders]. , 1979, Duodecim; laaketieteellinen aikakauskirja.
[8] F. Pope,et al. BIOCHEMICAL HETEROGENEITY OF OSTEOGENESIS IMPERFECTA: NEW VARIANT , 1979, The Lancet.
[9] V. McKusick,et al. The Marfan syndrome: diagnosis and management. , 1979, The New England journal of medicine.
[10] V. McKusick,et al. The Cardiovascular Aspects of Marfan's Syndrome: A Heritable Disorder of Connective Tissue , 1955, Circulation.