Authors:
Semina, EV
Brownell, I
Mintz-Hittner, HA
Murray, JC
Jamrich, M
Citation: Ev. Semina et al., Mutations in the human forkhead transcription factor FOXE3 associated withanterior segment ocular dysgenesis and cataracts, HUM MOL GEN, 10(3), 2001, pp. 231-236
Citation: Ev. Semina et al., Isolation and characterization of a novel human paired-like homeodomain-containing transcription factor gene, VSX1, expressed in ocular tissues, GENOMICS, 63(2), 2000, pp. 289-293
Citation: Ha. Mintz-hittner et Km. Fernandez, Successful amblyopia therapy initiated after age 7 years - Compliance curves, ARCH OPHTH, 118(11), 2000, pp. 1535-1541
Authors:
Mintz-Hittner, HA
Miyashiro, MJ
Knight-Nanan, DM
O'Malley, RE
Marlar, RA
Citation: Ha. Mintz-hittner et al., Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency, OPHTHALMOL, 106(8), 1999, pp. 1525-1530
Citation: Mj. Miyashiro et Ha. Mintz-hittner, Penetrating ocular injury with a fetal scalp monitoring spiral electrode, AM J OPHTH, 128(4), 1999, pp. 526-528