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:
Fulton, AB
Hansen, RM
Petersen, RA
Vanderveen, DK
Citation: Ab. Fulton et al., The rod photoreceptors in retinopathy of prematurity - An electroretinographic study, ARCH OPHTH, 119(4), 2001, pp. 499-505
Authors:
Lotery, AJ
Jacobson, SG
Fishman, GA
Weleber, RG
Fulton, AB
Namperumalsamy, P
Heon, E
Levin, AV
Grover, S
Rosenow, JR
Kopp, KK
Sheffield, VC
Stone, EM
Citation: Aj. Lotery et al., Mutations in the CRB1 gene cause Leber congenital amaurosis, ARCH OPHTH, 119(3), 2001, pp. 415-420
Citation: Rm. Hansen et Ab. Fulton, Background adaptation in children with a history of mild retinopathy of prematurity, INV OPHTH V, 41(1), 2000, pp. 320-324
Authors:
L'Ecuyer, TJ
Schutte, BC
Mendel, KA
Morris, E
Fulton, AB
Citation: Tj. L'Ecuyer et al., Muscle-specific transcription factors in fibroblasts expressing the alpha-striated tropomyosin 3 ' untranslated region, MOL GEN MET, 67(3), 1999, pp. 213-226
Authors:
Timmers, AM
Fox, DA
He, LH
Hansen, RM
Fulton, AB
Citation: Am. Timmers et al., Rod photoreceptor maturation does not vary with retinal eccentricity in mammalian retina, CURR EYE R, 18(6), 1999, pp. 393-402
Citation: Ab. Fulton, Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome) (vol 117, pg 251, 1999), ARCH OPHTH, 117(8), 1999, pp. 1099-1099
Citation: Ab. Fulton, Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome), ARCH OPHTH, 117(2), 1999, pp. 251-252