Zoekresultaten - Kathryn P. Burdon

Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome) door Shari Javadiyan, Jamie E. Craig, Shiwani Sharma, Karen M. Lower, Theresa Casey, Eric Haan, Emmanuelle Souzeau, Kathryn P. Burdon

Connect to this object online.

Human Lipoxygenase Pathway Gene Variation and Association with Markers of Subclinical Atherosclerosis in the Diabetes Heart Study door Kathryn P. Burdon, Megan E. Rudock, Allison B. Lehtinen, Carl D. Langefeld, Donald W. Bowden, Thomas C. Register, Yongmei Liu, Barry I. Freedman, J. Jeffrey Carr, Catherine C. Hedrick, Stephen S. Rich

Connect to this object online.

Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy door Patricia S. Graham, Georgia Kaidonis, Sotoodeh Abhary, Mark C. Gillies, Mark Daniell, Rohan W. Essex, John H. Chang, Stewart R. Lake, Bishwanath Pal, Alicia J. Jenkins, Alex W. Hewitt, Ecosse L. Lamoureux, Philip G. Hykin, Nikolai Petrovsky, Matthew A. Brown, Jamie E. Craig, Kathryn P. Burdon

Connect to this object online.