Was the Human Genome Project worth the effort? von Daiger, S.P.

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Localization of two genes for usher syndrome type I to chromosome 11 von Smith, Richard J.H., Lee, Elizabeth C., Kimberling, William J., Daiger, Stephen P., Pelias, Mary Z., Keats, Bronya J.B., Jay, Marcelle, Bird, Alan, Reardon, William, Guest, Mary, Ayyagari, Radha, Fielding Hejtmancik, J.

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Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites von Sohocki, Melanie M., Sullivan, Lori S., Harrison, Wilbur R., Sodergren, Erica J., Elder, Frederick F.B., Weinstock, George, Tanase, Sumio, Daiger, Stephen P.

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Nonsyndromic cleft lip and palate : no evidence of linkage to HLA or factor 13A von HECHT, J. T, YAPING WANG, CONNOR, B, BLANTON, S. H, DAIGER, S. P

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Localization and Characterization of the Human ADP-Ribosylation Factor 5 (ARF5) Gene von McGuire, Rachel E., Daiger, Stephen P., Green, Eric D.

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Evidence for genetic heterogeneity in tuberous sclerosis : one locus on chromosome 9 and at least one locus elsewhere von NORTHRUP, H, KWIATKOWSKI, D. J, ROACH, E. S, DOBYNS, W. B, LEWIS, R. A, HERMAN, G. E, RODRIGUEZ, E. JR, DAIGER, S. P, BLANTON, S. H

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Gen 2000;24:79–83 von Sohoki, M.M, Browne, S.J, Sullivan, L.S, Blackshaw, S, Cepko, C.L, Payne, A.M, Bhattacharya, S.S, Khaliq, S, Mehdi, S.Q, Birch, D.G, Harrison, W.R, Elder, F.F.B, Heckenlively, J.R, Daiger, S.P

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A new Sty l RFLP and haplotypes with the Hin dIII RFLP at the D8S5 (TL11) locus von Cottingham, A.W., Blanton, S.H., Retief, A.E., Warnich, L., Daiger, S.P.

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Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT) von SADLER, L. A, BLANTON, S. H, DAIGER, S. P

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Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E) von Sullivan, L.S., Parrish, J., Wagner, M.J., Wells, D., Blanton, S.H., Daiger, S.P.

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The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2 von Chan, L., VanTuinen, P., Ledbetter, D.H., Daiger, S.P., Gotto, A.M., Chen, S.H.

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Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis von Ni, Li, Wagner, Michael J., Kimberling, William J., Pembrey, Marcus E., Grundfast, Kenneth M., Kumar, Shrawan, Daiger, Stephen P., Wells, Dan E., Johnson, Kristin, Smith, Richard J. H.

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Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q von Blanton, S.H., Cottingham, A.W., Giesenschlag, N., Heckenlively, J.R., Humphries, P., Daiger, S.P.

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A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL 11) locus von COTTINGHAM, A. W, BLANTON, S. H, RETIEF, A. E, WARNICH, L, DAIGER, S. P

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A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13 von Cottingham, A.W., Sadler, L.A., BIanton, S.H., Wagner, M.J, Weils, D.E., Heckenlively, J.R., Daiger, S.P.

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Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis von Zoghbi, H.Y., Sandkuyl, L.A., Ott, J., Daiger, S.P., Pollack, M.S., O'Brien, W.E., Beaudet, A.L.

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