Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis) von Doherty, D, Parisi, M A, Finn, L S, Gunay-Aygun, M, Al-Mateen, M, Bates, D, Clericuzio, C, Demir, H, Dorschner, M, van Essen, A J, Gahl, W A, Gentile, M, Gorden, N T, Hikida, A, Knutzen, D, Özyurek, H, Phelps, I, Rosenthal, P, Verloes, A, Weigand, H, Chance, P F, Dobyns, W B, Glass, I A

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AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome von Parisi, M A, Doherty, D, Eckert, M L, Shaw, D W W, Ozyurek, H, Aysun, S, Giray, O, Al Swaid, A, Al Shahwan, S, Dohayan, N, Bakhsh, E, Indridason, O S, Dobyns, W B, Bennett, C L, Chance, P F, Glass, I A

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Expression of SHOX in Human Fetal and Childhood Growth Plate von Munns, C. J. F., Haase, H. R., Crowther, L. M., Hayes, M. T., Blaschke, R., Rappold, G., Glass, I. A., Batch, J. A.

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Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy von Lehman, A.M., Eydoux, P., Doherty, D., Glass, I.A., Chitayat, D., Chung, B.Y.H., Langlois, S., Yong, S.L., Lowry, R.B., Hildebrandt, F., Trnka, P.

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The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda von Gedeon, A.K., Tiller, G.E., Le Merrer, M., Heuertz, S., Tranebjaerg, L., Chitayat, D., Robertson, S., Glass, I.A., Savarirayan, R., Cole, W.G., Rimoin, D.L., Kousseff, B.G., Ohashi, H., Zabel, B., Munnich, A., Gecz, J., Mulley, J.C.

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Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis von Moloney, DM, Wall, SA, Ashworth, GJ, Oldridge, M, Glass, IA, Francomano, CA, Muenke, M, Wilkie, AOM

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Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures von BENNETT, C. L, HUYNH, H. M, CHANCE, P. F, GLASS, I. A, GOSPE, S. M

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Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements von Souter, V. L., Glass, I. A., Chapman, D. B., Raff, M. L., Parisi, M. A., Opheim, K. E., Disteche, C. M.

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Trisomy of the short stature homeobox‐containing gene (SHOX), resulting from a duplication‐deletion of the X chromosome von Adamson, K. A., Cross, I., Batch, J. A., Rappold, G. A., Glass, I. A., Ball, S. G.

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X linked mental retardation von Glass, I A

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Prenatal diagnosis of dominant dystrophic epidermolysis bullosa, by COL7A1 molecular analysis von Klingberg, S., Mortimore, R., Parkes, J., Chick, J. E. D., Clague, A. E., Murrell, D., Weedon, D., Glass, I. A.

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Cbfa1-Independent Decrease in Osteoblast Proliferation, Osteopenia, and Persistent Embryonic Eye Vascularization in Mice Deficient in Lrp5, a Wnt Coreceptor von Kato, Masaki, Patel, Millan S, Levasseur, Regis, Lobov, Ivan, Chang, Benny H-J, Glass, 2nd, Donald A, Hartmann, Christine, Li, Lan, Hwang, Tae-Ho, Brayton, Cory F, Lang, Richard A, Karsenty, Gerard, Chan, Lawrence

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Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood von Flanagan, S F, Munns, C F J, Hayes, M, Williams, B, Berry, M, Vickers, D, Rao, E, Rappold, G A, Batch, J A, Hyland, V J, Glass, I A

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Congenital Erythropoietic Porphyria: Prolonged High-Level Expression and Correction of the Heme Biosynthetic Defect by Retroviral-Mediated Gene Transfer into Porphyric and Erythroi... von Kauppinen, R., Glass, I.A., Aizencang, G., Astrin, K.H., Atweh, G.F., Desnick, R.J.

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Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome von Glass, I A, Good, P, Coleman, M P, Fullwood, P, Giles, M G, Lindsay, S, Nemeth, A H, Davies, K E, Willshaw, H A, Fielder, A

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Low Maternal Serum Oestriol at Mid-Trimester May Indicate a Fetal Disorder of Cholesterol Biosynthesis von Craig MBBS, J.E., Savage MSc, V., Cowley FRCPA, D., Clague FRCPA, A., Glass MD, LA

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Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome von SUTHERS, G. K, MULLEY, J. C, HAITES, N. E, OOSTRA, B. A, GINE, R, CARBALLO, M, MORRIS, C. P, HOPWOOD, J. J, SUTHERLAND, G. R, VOELCKEL, M. A, DAHL, N, VÄISÄNEN, M. L, STEINBACH, P, GLASS, I. A, SCHWARTZ, C. E, VAN OOST, B. A, THIBODEAU, S. N

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Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments von GLASS, I. A, PASSAGE, M, BERNATOWICZ, L, SALIDO, E. C, MOHANDAS, T, YEN, P. H, SHAPIRO, L. J

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Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase von Glass, I A, Swindlehurst, C A, Aitken, D A, McCrea, W, Boyd, E

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HUMAN FETAL TISSUE DONATION: ABORTION PATIENT EXPERIENCE AND PERSPECTIVES von Cort, LA, Dempsey, JC, MacDuffie, K, Glass, IA, Benson, LS

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