Mutations in NPC1 Highlight a Conserved NPC1-Specific Cysteine-Rich Domain by Greer, WL, Dobson, MJ, Girouard, GS, Byers, DM, Riddell, DC, Neumann, PE

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Linkage of Niemann-Pick Disease Type D to the Same Region of Human Chromosome 18 as Niemann-Pick Disease Type C by Greer, W.L., Riddell, D.C., Byers, D.M., Welch, J.P., Girouard, G.S., Sparrow, S.M., Gillan, T.L., Neumann, P.E.

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The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097→T transversion in NPC1 by GREER, W. L, RIDDELL, D. C, GILLAN, T. L, GIROUARD, G. S, SPARROW, S. M, BYERS, D. M, DOBSON, M. J, NEUMANN, P. E

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Associations between genetic polymorphisms of Phase I and II metabolizing enzymes, p53 and susceptibility to esophageal adenocarcinoma by Casson, A.G, Zheng, Z, Chiasson, D, MacDonald, K, Riddell, D.C, Guernsey, J.R, Guernsey, D.L, McLaughlin, J

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Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype by De Becker, I, Riddell, D C, Dooley, J M, Tremblay, F

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Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease by Greer, WL, Riddell, DC, Murty, S, Gillan, TL, Girouard, GS, Sparrow, SM, Tatlidil, C, Dobson, MJ, Neumann, PE

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Absence of fragile X syndrome in Nova Scotia by BERESFORD, R G, TATLIDIL, C, RIDDELL, D C, WELCH, J P, LUDMAN, M D, NEUMANN, P E, GREER, W L

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A gene family in Drosophila melanogaster coding for trypsin-like enzymes by Davis, Claytus A., Riddell, D.Christie, Higgins, Michael J., Holden, Jeanette J.A., White, Bradley N.

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Fabry disease in a large Nova Scotia kindred: carrier detection using leucocyte alpha-galactosidase activity and an NcoI polymorphism detected by an alpha-galactosidase cDNA clone by Kirkilionis, A J, Riddell, D C, Spence, M W, Fenwick, R G

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ING1 and p53 tumor suppressor gene alterations in adenocarcinomas of the esophagogastric junction by Hara, Yasuo, Zheng, Zuoyu, Evans, Susan C, Malatjalian, Dickran, Riddell, D.Christie, Guernsey, Duane L, Wang, Li Dong, Riabowol, Karl, Casson, Alan G

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Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7 by STARR, T, WOOD, S, RIDDELL, D. C, HAMERTON, J. L

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Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor by RIDDELL, D. C, MALLONEE, R, PHILLIPS, J. A, PARKS, J. S, SEXTON, L. A, HAMERTON, J. L

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Corneal Clouding Complicating a Corneal Transplant by Riddell, Jeffrey C., MD, Burg, Michael D., MD, FACEP

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Establishment and characterization of a renal cell carcinoma line from a patient with von Hippel-Lindau syndrome by Morash, Barbara A., Lee, Christine L.Y., Rowden, Geoffrey, Riddell, D.Christie, Guernsey, Duane L.

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A Content Analysis of Kindergarten-12th Grade School-based Nutrition Interventions: Taking Advantage of Past Learning by Roseman, Mary G., PhD, RD, LD, Riddell, Martha C., DrPH, RD, Haynes, Jessica N., MS, RD, LD

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THE SOUTHLAND FLOOD OF JANUARY 1984 (NOTE) by Riddell, D. C.

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FLOOD HYDROLOGY OF THE MOTU RIVER by Riddell, D. C.

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Structural analysis of the three vitellogenin genes in Drosophila melanogaster by Riddell, D.C, Higgins, M.J, McMillan, B.J, White, B.N

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Investigation of physical and hydrological characteristics of the Lismore stony silt loam by Riddell, D. C

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Association between Breus' mole and partial hydatidiform mole: chance or can hydropic villi precipitate placental massive subchorionic thrombosis? by Kim, Dae Tong, Riddell, D Christie, Welch, J Philip, Scott, Heather, Fraser, Robert B, Wright, Jr, James R

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