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Ophthalmic Genetics|December 29, 2004
Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesisS M Quinn, G C M Black, S Biswas, et al.
Ophthalmic Genetics|March 18, 2006
A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosisH Abouzeid, Y Li, I H Maumenee, et al.
Ophthalmic Genetics|January 23, 1999
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotypeV Ponjavic, S Andréasson, M Abrahamson, et al.
Ophthalmic Genetics|January 23, 1999
Analysis of the IRBP gene as a cause of RP in 45 ARRP Spanish families. Autosomal recessive retinitis pigmentosa. Interstitial retinol binding protein. Spanish Multicentric and Multidisciplinary Group for Research into Retinitis PigmentosaD Valverde, F Vázquez-Gundín, E del Rio, et al.
Ophthalmic Genetics|January 23, 1999
Coloboma of the lens, optic nerve hypoplasia, and orbital hemangioma--a possible developmental field defectA K Fard, E I Traboulsi
Ophthalmic Genetics|December 1, 1995
Molecular analysis and predictive testing in retinoblastomaD R Lohmann, B Brandt, U Oehlschläger, et al.
Ophthalmic Genetics|December 1, 1995
Orbital rhabdomyosarcoma: treatment or overtreatmentC M Notis, D H Abramson, R H Sagerman, et al.
Ophthalmic Genetics|December 1, 1995
A family with a syndrome of ectopia lentis, spontaneous filtering blebs, and craniofacial dysmorphismS Shawaf, B Noureddin, A Khouri, et al.
Ophthalmic Genetics|December 1, 1995
Duane retraction syndrome associated with Rubinstein-Taybi syndromeO A Cruz, D M Mason, M S Eswara, et al.
Ophthalmic Genetics|November 12, 1998
The two-stage mutation model in retinal hemangioblastomaJ H Chang, C W Spraul, M L Lynn, et al.
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