Monzer Jabak

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

Bassem A. Bejjani, Richard A. Lewis, Karim F. Tomey et al. · The American Journal of Human Genetics · 1998 · 319 citations · Full text

Ocular Disease, Ophthalmology, Genetic Disorder +9

Congenital Fibrosis of the Extraocular Muscles Type 2, an Inherited Exotropic Strabismus Fixus, Maps to Distal 11q13

S.M. Wang, Johan Zwaan, Paul B. Mullaney et al. · The American Journal of Human Genetics · 1998 · 99 citations · Full text

Rare Diseases, Congenital Fibrosis, Medicine +5

A novel locus for Leber congenital amaurosis on chromosome 14q24

David W. Stockton, Richard A. Lewis, Emad B. Abboud et al. · Human Genetics · 1998 · 80 citations

Developmental Biology, Genetic Disorder, Genetics +6

Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in <i>RLBP1</i>

Nicholas Katsanis, Lewis Ra, JC Cavender et al. · Clinical Genetics · 2001 · 70 citations

Workup for Metastatic Retinoblastoma

Zeynel A. Karcioglu, Saleh A. Al-Mesfer, Emad B. Abboud et al. · Ophthalmology · 1997 · 67 citations

Ophthalmology, Medicine, Metastatic Retinoblastoma +4