© 2012
Publications in 2008
Giunta C, Elçioglu NH, Albrecht B, Eich G, Chambaz C, Janecke AR, Yeowell H, Weis MA, Eyre DR, Kraenzlin M, Steinmann B. Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome – An autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13. Am. J. Hum. Genet. 2008; 82(6), 1290-1305. PubMed
Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, Pepin MG, Weis MA, Eyre DR, Walsh J, Lambert D, Green A, Robinson H, Michelson M, Houge G, Lindman C, Martin J, Ward J, Lemyre E, Mitchell JJ, Krakow D, Rimoin DL, Cohn DH, Byers PH, Lee B. CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta. Hum. Mutat. 2008; 29(12):1435-1442. PubMed
Seegmiller RE, Bomsta BD, Bridgewater LC, Niederhauser CM, Montaño C, Sudweeks S, Eyre DR, Fernandes RJ. The Heterozygous Disproportionate micromelia (Dmm) mouse: Morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype. J. Histochem. Cytochem. 2008; 56(11), 1003-1011. PubMed
Hunter DJ, LaValley M, Li J, Bauer DC, Nevitt M, DeGroot J, Poole R, Eyre D, Guermazi A, Gale D, Totterman S, Felson DT. Biochemical markers of bone turnover and their association with bone marrow lesions. Arthritis Res. Ther. 2008; 10(4), R102. PubMed
Eyre DR, Weis MA, Wu JJ. Advances in collagen cross-link analysis. Methods 2008; 45: 65-74. PubMed
