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Results: 1-4 |
Results: 4

Authors: Nishimura, DY Searby, CC Carmi, R Elbedour, K Van Maldergem, L Fulton, AB Lam, BL Powell, BR Swiderski, RE Bugge, KE Haider, NB Kwitek-Black, AE Ying, LH Duhl, DM Gorman, SW Heon, E Iannaccone, A Bonneau, D Biesecker, LG Jacobson, SG Stone, EM Sheffield, VC
Citation: Dy. Nishimura et al., Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2), HUM MOL GEN, 10(8), 2001, pp. 865-874

Authors: Sheffield, VC Ying, LH Carmi, R Landau, D
Citation: Vc. Sheffield et al., Complement factor h gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome - Reply to Buddles et al., AM J HU GEN, 66(5), 2000, pp. 1722-1722

Authors: Swiderski, RE Ying, LH Cassell, MD Alward, WLM Stone, EM Sheffield, VC
Citation: Re. Swiderski et al., Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brain, MOL BRAIN R, 68(1-2), 1999, pp. 64-72

Authors: Ying, LH Katz, Y Schlesinger, M Carmi, R Shalev, H Haider, N Beck, G Sheffield, VC Landau, D
Citation: Lh. Ying et al., Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome, AM J HU GEN, 65(6), 1999, pp. 1538-1546
Risultati: 1-4 |