Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25 von Mirzayans, Farideh, Gould, Douglas B, Héon, E, Billingsley, Gail D, Cheung, Jason C, Mears, Alan J, Walter, Michael A

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The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer von Héon, Elise, Priston, Megan, Schorderet, Daniel F., Billingsley, Gail D., Girard, Philippe Othenin, Lubsen, Nicolette, Munier, Francis L.

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Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25 von Mirzayans, F, Gould, D B, Héon, E, Billingsley, G D, Cheung, J C, Mears, A J, Walter, M A

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Physical mapping of four serpin genes α1-antitrypsin, α1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome 14q32.1 von BILLINGSLEY, G. D, WALTER, M. A, HAMMOND, G. L, COX, D. W

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Physical and genetic mapping of the serpin gene cluster at 14q32.1 : allelic association and a unique haplotype associated with α1-antitrypsin deficiency von BYTH, B. C, BILLINGSLEY, G. D, COX, D. W

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Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome6p25 von Mirzayans, Farideh, Gould, Douglas B, Heon, E, Billingsley, Gail D, Cheung, Jason C, Mears, Alan J, Walter, Michael A

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Functional assessment of genetic variants of ?1-Antitrypsin von Billingsley, Gail D., Cox, Diane Wilson

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Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene von Vincent, Andrea L., Billingsley, Gail, Buys, Yvonne, Levin, Alex V., Priston, Megan, Trope, Graham, Williams-Lyn, Donna, Héon, Elise

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Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization von Di Scipio, Matteo, Tavares, Erika, Deshmukh, Shriya, Audo, Isabelle, Green-Sanderson, Kit, Zubak, Yuliya, Zine-Eddine, Fayçal, Pearson, Alexander, Vig, Anjali, Tang, Chen Yu, Mollica, Antonio, Karas, Jonathan, Tumber, Anupreet, Yu, Caberry W, Billingsley, Gail, Wilson, Michael D, Zeitz, Christina, Héon, Elise, Vincent, Ajoy

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Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population von Billingsley, Gail, Bin, Jenea, Fieggen, Karen J, Duncan, Jacque L, Gerth, Christina, Ogata, Koji, Wodak, Shoshana S, Traboulsi, Elias I, Fishman, Gerald A, Paterson, Andrew, Chitayat, David, Knueppel, Tanja, Millán, José M, Mitchell, Grant A, Deveault, Catherine, Héon, Elise

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CRYBA4, a Novel Human Cataract Gene, Is Also Involved in Microphthalmia von Billingsley, Gail, Santhiya, Sathiyavedu T., Paterson, Andrew D., Ogata, Koji, Wodak, Shoshana, Hosseini, S. Mohsen, Manisastry, Shyam Manohar, Vijayalakshmi, Perumalsamy, Gopinath, Pudhiya Mundyat, Graw, Jochen, Héon, Elise

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Cetuximab Combined With Induction Oxaliplatin and Capecitabine, Followed by Neoadjuvant Chemoradiation for Locally Advanced Rectal Cancer: SWOG 0713 von Leichman, Cynthia Gail, McDonough, Shannon L., Smalley, Stephen R., Billingsley, Kevin G., Lenz, Heinz-Josef, Beldner, Matthew A., Hezel, Aram F., Velasco, Mario R., Guthrie, Katherine A., Blanke, Charles D., Hochster, Howard S.

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OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium von Vincent, Ajoy, Forster, Nicole, Maynes, Jason T, Paton, Tara A, Billingsley, Gail, Roslin, Nicole M, Ali, Arfan, Sutherland, Joanne, Wright, Tom, Westall, Carol A, Paterson, Andrew D, Marshall, Christian R, Héon, Elise

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VSX1: A gene for posterior polymorphous dystrophy and keratoconus von Héon, Elise, Greenberg, Alex, Kopp, Kelly K., Rootman, David, Vincent, Andrea L., Billingsley, Gail, Priston, Megan, Dorval, Kimberley M., Chow, Robert L., McInnes, Roderick R., Heathcote, Godfrey, Westall, Carol, Sutphin, John E., Semina, Elena, Bremner, Rod, Stone, Edwin M.

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Genetic Heterogeneity of the Coppock-like Cataract: A Mutation in CRYBB2 on Chromosome 22q11.2 von Gill, Dan, Klose, Robert, Munier, Francis L, McFadden, Michelle, Priston, Megan, Billingsley, Gail, Ducrey, Nicolas, Schorderet, Daniel F, Heon, Elise

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Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly von Vincent, Andrea, Billingsley, Gail, Priston, Megan, Williams-Lyn, Donna, Sutherland, Joanne, Glaser, Tom, Oliver, Edward, Walter, Michael A, Heathcote, Godfrey, Levin, Alex, Héon, Elise

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A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22 von Héon, Elise, Paterson, Andrew D., Fraser, Michael, Billingsley, Gail, Priston, Megan, Balmer, Aubin, Schorderet, Daniel F., Verner, Andrei, Hudson, Thomas J., Munier, Francis L.

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Gene Localization for Aculeiform Cataract, on Chromosome 2q33-35 von Héon, Elise, Liu, Sen, Billingsley, Gail, Bernasconi, Ottavio, Tsifildis, Cathy, Schorderet, Daniel F., Munier, Francis L.

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