Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness von Bech-Hansen, N. Torben, Naylor, Margaret J., Maybaum, Tracy A., Pearce, William G., Koop, Ben, Fishman, Gerald A., Mets, Marilyn, Musarella, Maria A., Boycott, Kym M.

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Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F von Boycott, Kym M., PhD, Pearce, William G., MD, Bech-Hansen, N. Torben, PhD

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Tracking ability in subjects symptomatic of cumulative trauma disorder: does it relate to disability? von Brouwer, Brenda, Mazzoni, ClÁudia, William Pearce, G.

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Tephrochronology, magnetostratigraphy and mammalian faunas of Middle and Early Pleistocene sediments at two sites on the Old Crow River, northern Yukon Territory, Canada von Westgate, John A., Pearce, G. William, Preece, Shari J., Schweger, Charles E., Morlan, Richard E., Pearce, Nicholas J.G., Perkins, T. William

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Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23 von BECH-HANSEN, N. T, BOYCOTT, K. M, GRATTON, K. J, ROSS, D. A, FIELD, L. L, PEARCE, W. G

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Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome von Kulak, Stephen C., Kozlowski, Kathy, Semina, Elena V., Pearce, William G., Walter, Michael A.

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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants von BOYCOTT, Kym M, MAYBAUM, Tracy A, NAYLOR, Margaret J, WELEBER, Richard G, ROBITAILLE, Johane, MIYAKE, Yozo, BERGEN, Arthur A. B, PIERPONT, Mary Ella, PEARCE, William G, BECH-HANSEN, N. Torben

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Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25 von MEARS, A. J, MIRZAYANS, F, GOULD, D. B, PEARCE, W. G, WALTER, M. A

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Autosomal Dominant Axenfeld-Rieger Anomaly Maps to 6p25 von GOULD, DOUGLAS B., PEARCE, WILLIAM G., WALTER, MICHAEL A.

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Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness von Boycott, Kym M., Pearce, William G., Musarella, Maria A., Weleber, Richard G., Maybaum, Tracy A., Birch, David G., Miyake, Yozo, Young, Rockefeller S.L., Bech-Hansen, N. Torben

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Testing market segment acceptance of new designs of industrial services von Woodside, Arch G., Pearce, William G.

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Autosomal-dominant Iridogoniodysgenesis and Axenfeld-Rieger Syndrome are Genetically Distinct von Walter, Michael A., Mirzayans, Farideh, Mears, Alan J., Hickey, Kristin, Pearce, William G.

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Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning von Mirzayans, Farideh, Mears, Alan J., Guo, Sun-Wei, Pearce, William G., Walter, Michael A.

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Autosomal Dominant Axenfeld‐Rieger Anomaly Maps to 6p25 von Gould, Douglas B., Mears, Alan J., Pearce, William G., Walter, Michael A.

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Loss-of-function mutations in a calcium-channel α 1 -subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness von Mets, Marilyn, Maybaum, Tracy A, Pearce, William G, Musarella, Maria A, Naylor, Margaret J, Bech-Hansen, N. Torben, Boycott, Kym M, Fishman, Gerald A, Koop, Ben

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Histopathology and molecular basis of iridogoniodysgenesis syndrome von Pearce, William G., Mielke, Bruce, Kulak, Stephen C., Walter, Michael A.

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Inherited Iridogoniodysgenesis von MacDonald, Ian M., Pearce, William G.

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Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7 von Bech-Hansen, N.Torben, Moore, Brenda J., Pearce, William G.

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Testing Market Segment Acceptance of New Designs of Industrial Services von Woodside, Arch G., Pearce, William G.

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Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness von Clarke, M P, Sullivan, T J, Francis, C, Baumal, R, Fenton, T, Pearce, W G

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