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1 Telangiectasia, Hereditary Hemorrhagic. : Living with HHT : understanding and managing your hereditary hemorrhagic telangiectasia / Sara Palmer, Ph.D  2017 1
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Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber -- See Telangiectasia, Hereditary Hemorrhagic


An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
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Telangiectasia, Hereditary Hemorrhagic, Type 1 -- See Telangiectasia, Hereditary Hemorrhagic


An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
  1
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