A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13 von Guru, Siradanahalli C., Olufemi, Shodimu-Emmanuel, Manickam, Pachiappan, Cummings, Christiano, Gieser, Linn M., Pike, Brian L., Bittner, Michael L., Jiang, Yuan, Chinault, A.Craig, Nowak, Norma J., Brzozowska, Anna, Crabtree, Judy S., Wang, Yingping, Roe, Bruce A., Weisemann, Jane M., Boguski, Mark S., Agarwal, Sunita K., Burns, A.Lee, Spiegel, Allen M., Marx, Stephen J., Flejter, Wendy L., de Jong, Pieter J., Collins, Francis S., Chandrasekharappa, Settara C.

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Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa von Friedman, J, Ray, JW, Waseem, N, Johnson, K, Brooks, MJ, Hugosson, T, Breuer, D, Branham, KE, Krauth, DS, Browne, SJ, Ponjavic, V, Granse, L, Khanna, R, Trager, EH, Gieser, LM, Hughbanks-Wheaton, D, Cojocaru, RI, Ghiasvand, NM, Chakarova, C, Abrahamson, M, Goring, HHH, Webster, AR, Birch, DG, Abecasis, GR, Fann, Y, Bhattacharya, SS, Daiger, SP, Heckenlively, JR, Andreasson, S, Swaroop, A

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Heterozygous Triplication of Upstream Regulatory Sequences Leads to Dysregulation of Matrix Metalloproteinase 19 in Patients with Cavitary Optic Disc Anomaly von Hazlewood, Ralph J., Roos, Benjamin R., Solivan-Timpe, Frances, Honkanen, Robert A., Jampol, Lee M., Gieser, Stephen C., Meyer, Kacie J., Mullins, Robert F., Kuehn, Markus H., Scheetz, Todd E., Kwon, Young H., Alward, Wallace L.M., Stone, Edwin M., Fingert, John H.

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