Autosomal Recessive CHED Associated With Novel Compound Heterozygous Mutations in SLC4A11 von Aldave, Anthony J, Yellore, Vivek S, Bourla, Nirit, Momi, Rominder S, Khan, M Ali, Salem, Andrew K, Rayner, Sylvia A, Glasgow, Ben J, Kurtz, Ira

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Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy von Yellore, Vivek S, Khan, M Ali, Bourla, Nirit, Rayner, Sylvia A, Chen, Michael C, Sonmez, Baris, Momi, Rominder S, Sampat, Kapil M, Gorin, Michael B, Aldave, Anthony J

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No Pathogenic Mutations Identified in the COL8A2 Gene or Four Positional Candidate Genes in Patients with Posterior Polymorphous Corneal Dystrophy von Yellore, Vivek S, Rayner, Sylvia A, Emmert-Buck, Leslie, Tabin, Geoffrey C, Raber, Irving, Hannush, Sadeer B, Stulting, R. Doyle, Sampat, Kapil, Momi, Rominder, Principe, Alexandre H, Aldave, Anthony J

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A longitudinal prospective study of pediatric patients with Inflammatory Bowel Disease (IBD) using cytogenetic and immunological markers von Heyman, Melvin B., Harmatz, Paul, Golden, Daniel W., Duramad, Paurene, Bae, Jin, Cooper, Jennifer, Momi, Rominder, Chen, Connie, Hubbard, Alan E., Holland, Nina T.

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