Zobrazeno 1 - 2
of 2
pro vyhledávání: '"C. Eugene Jackson"'
Autor:
Mary L. Warner, Joshua D. Smith, C.J.J. Westermann, Carol J. Gallione, Kimberly A. McAllister, Timothy T. Stenzel, Kara B. Anthony, York E. Miller, Douglas A. Marchuk, William J. Craigen, Eric Y. Yeh, Jonathan Berg, C. Eugene Jackson, Melanie A. Baldwin, Calvin P.H. Vary, Alan E. Guttmacher, Andreas Lux, Yan Xue, Daniel J. Klaus
Publikováno v:
Human Mutation. 11:286-294
Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by multisystemic vascular dysplasia and recurrent hemorrhage from the sites of vascular lesions. Two genes have been identified for HHT. Endoglin, a TGF-β bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08794d1227030cb3c88780bf0541920d
https://doi.org/10.1002/(sici)1098-1004(1998)11:4<286::aid-humu6>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1998)11:4<286::aid-humu6>3.0.co
Autor:
Carol J. Gallione, Daniel J. Klaus, Eric Y. Yeh, Timothy T. Stenzel, Yan Xue, Kara B. Anthony, Kimberly A. McAllister, Melanie A. Baldwin, Jonathan N. Berg, Andreas Lux, Joshua D. Smith, Calvin P.H. Vary, William J. Craigen, C.J.J. Westermann, Mary L. Warner, York E. Miller, C. Eugene Jackson, Alan E. Guttmacher, Douglas A. Marchuk
Publikováno v:
Human Mutation. 11:286-294
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74baf252e864ce4130d43d96658ee28a
https://doi.org/10.1002/(sici)1098-1004(1998)11:4<286::aid-humu6>3.3.co
https://doi.org/10.1002/(sici)1098-1004(1998)11:4<286::aid-humu6>3.3.co