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