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Results:
1-7
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Results: 7
Homozygous mutations in ARIX (PHOX2A) result in congenital fibrosis of theextraocular muscles type 2
Authors:
Nakano, M
Yamada, K
Fain, J
Sener, EC
Selleck, CJ
Awad, AH
Zwaan, J
Mullaney, PB
Bosley, TM
Engle, EC
Citation: M. Nakano et al., Homozygous mutations in ARIX (PHOX2A) result in congenital fibrosis of theextraocular muscles type 2, NAT GENET, 29(3), 2001, pp. 315-320
Authors:
Flaherty, MP
Grattan-Smith, P
Steinberg, A
Jamieson, R
Engle, EC
Citation: Mp. Flaherty et al., Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia, OPHTHALMOL, 108(7), 2001, pp. 1313-1322
Authors:
Shivaram, SM
Engle, EC
Petersen, RA
Robb, RM
Citation: Sm. Shivaram et al., Congenital fibrosis syndromes, INT OPHTH C, 41(4), 2001, pp. 105-113
A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12
Authors:
Sener, EC
Lee, BA
Turgut, B
Akarsu, AN
Engle, EC
Citation: Ec. Sener et al., A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12, ARCH OPHTH, 118(8), 2000, pp. 1090-1097
Authors:
Traboulsi, EI
Lee, BA
Mousawi, A
Khamis, AR
Engle, EC
Citation: Ei. Traboulsi et al., Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles, AM J OPHTH, 129(5), 2000, pp. 658-662
Authors:
Doherty, EJ
Macy, ME
Wang, SM
Dykeman, CP
Melanson, MT
Engle, EC
Citation: Ej. Doherty et al., CFEOM3: A new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3, INV OPHTH V, 40(8), 1999, pp. 1687-1694
Authors:
Engle, EC
Citation: Ec. Engle, The genetics of strabismus: Duane, Mobius, and fibrosis syndromes, OX MG MED G, (36), 1998, pp. 477-512
Risultati:
1-7
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