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Results: 1-5 |
Results: 5

Authors: Chang-Godinich, A Ades, S Schenkein, D Brooks, D Stambolian, D Raizman, MB
Citation: A. Chang-godinich et al., Lens changes in hereditary hyperferritinemia-cataract syndrome, AM J OPHTH, 132(5), 2001, pp. 786-788

Authors: Heath, S Robledo, R Beggs, W Feola, G Parodo, C Rinaldi, A Contu, L Dana, D Stambolian, D Siniscalco, M
Citation: S. Heath et al., A novel approach to search for identity by descent in small samples of patients and controls from the same Mendelian breeding unit: A pilot study on myopia, HUMAN HERED, 52(4), 2001, pp. 183-190

Authors: Kolosha, V Anoia, E de Cespedes, C Gitzelmann, R Shih, L Casco, T Saborio, M Trejos, R Buist, N Tedesco, T Skach, W Mitelmann, O Ledee, D Huang, K Stambolian, D
Citation: V. Kolosha et al., Novel mutations in 13 probands with galactokinase deficiency, HUM MUTAT, 15(5), 2000, pp. 447-453

Authors: Ai, YJ Zheng, Z O'Brien-Jenkins, A Bernard, DJ Wynshaw-Boris, T Ning, C Reynolds, R Segal, S Huang, K Stambolian, D
Citation: Yj. Ai et al., A mouse model of galactose-induced cataracts, HUM MOL GEN, 9(12), 2000, pp. 1821-1827

Authors: Hodes, ME Woodward, K Spinner, NB Emanuel, BS Enrico-Simon, A Kamholz, J Stambolian, D Zackai, EH Pratt, VM Thomas, IT Crandall, K Dlouhy, SR Malcolm, S
Citation: Me. Hodes et al., Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome, AM J HU GEN, 67(1), 2000, pp. 14-22
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