Marfan Syndrome is a hereditary disorder of connective tissue which primarily affects the cardiovascular, skeletal, and ocular systems. Remarkable progress in the field has been made in both clinical and basic-science research since the discovery of the gene for fibrillin-1 (FBN1) in 1991, mutations in which cause the Marfan syndrome. "Marfan ...
Marfan syndrome is a hereditary disorder of connective tissue which primarily affects the eyes, skeleton, blood vessels and various structures of the heart. Since 1943, when the cardiovascular manifestations of Marfan syndrome were first described, understanding of its nature, diagnostic tools, and surgical treatment have been remarkably improved. ...
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