A Late Presentation of a Fatal Disease: Juvenile Hemochromatosis

por Cherfane, Cynthia, Lee, Pauline, Guerin, Leana, Brown, Kyle
Publicado 2013

Genetic polymorphisms and susceptibility to lung disease

por Lee, Pauline L, West, Carol, Crain, Karen, Wang, Lei
Publicado 2006

Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension

por Bertoli, Luigi F., Lee, Pauline L., Lallone, Lauren, Barton, James C.
Publicado 2017

Exome Analysis Identified a Novel Mutation in the RBP4 Gene in a Consanguineous Pedigree with Retinal Dystrophy and Developmental Abnormalities

por Cukras, Catherine, Gaasterland, Terry, Lee, Pauline, Gudiseva, Harini V., Chavali, Venkata R. M., Pullakhandam, Raghu, Maranhao, Bruno, Edsall, Lee, Soares, Sandra, Reddy, G. Bhanuprakash, Sieving, Paul A., Ayyagari, Radha
Publicado 2012

Investigating the Molecular Basis of Retinal Degeneration in a Familial Cohort of Pakistani Decent by Exome Sequencing

por Maranhao, Bruno, Biswas, Pooja, Gottsch, Alexander D. H., Navani, Mili, Naeem, Muhammad Asif, Suk, John, Chu, Justin, Khan, Sheen N., Poleman, Rachel, Akram, Javed, Riazuddin, Sheikh, Lee, Pauline, Riazuddin, S. Amer, Hejtmancik, J. Fielding, Ayyagari, Radha
Publicado 2015