VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families von Bourassa, Cynthia V., Meijer, Inge A., Merner, Nancy D., Grewal, Kanwal K., Stefanelli, Mark G., Hodgkinson, Kathleen, Ives, Elizabeth J., Pryse-Phillips, William, Jog, Mandar, Boycott, Kym, Grimes, David A., Goobie, Sharan, Leckey, Richard, Dion, Patrick A., Rouleau, Guy A.

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Subscapularis tendon tears: A common sonographic finding in symptomatic postarthroplasty shoulders von Ives, Elizabeth P., Nazarian, Levon N., Parker, Laurence, Garrigues, Grant E., Williams, Gerald R.

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Independent Predictors of Acute Appendicitis on CT with Pathologic Correlation von Ives, Elizabeth P., MD, Sung, Susan, MD, McCue, Peter, MD, Durrani, Haroon, MD, Halpern, Ethan J., MD

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A transcriptional insulator at the imprinted H19/Igf2 locus von Kaffer, C R, Srivastava, M, Park, K Y, Ives, E, Hsieh, S, Batlle, J, Grinberg, A, Huang, S P, Pfeifer, K

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Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm von Telenius, Håkan, Kremer, Berry, Goldberg, Y. Paul, Theilmann, Jane, Andrew, Susan E, Zeisler, Jutta, Adam, Shelin, Greenberg, Cheryl, Ives, Elizabeth J, Clarke, Lorne A, Hayden, Michael R

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Myoglobin Catalyzes Its Own Nitration von Bourassa, James L, Ives, Elizabeth P, Marqueling, Ann L, Shimanovich, Roman, Groves, John T

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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 von DOUCETTE, Lance, MERNER, Nancy D, GREEN, Jane S, WILCOX, Edward R, SHOTLAND, Larry, LI, X. C, LEE, Ming, KING, Mary-Claire, YOUNG, Terry-Lynn, COOKE, Sandra, IVES, Elizabeth, GALUTIRA, Dante, WALSH, Vanessa, WALSH, Tom, MACLAREN, Linda, CATER, Tracey, FERNANDEZ, Bridget

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Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan von Ahmed, Zubair M, Li, Xiaoyan Cindy, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward R

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Quantitative Computed Tomography Perfusion of Prostate Cancer: Correlation with Whole-Mount Pathology von Ives, Elizabeth P., Burke, Melissa A., Edmonds, Pamela R., Gomella, Leonard G., Halpern, Ethan J.

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome von Weksberg, Rosanna, Shuman, Cheryl, Caluseriu, Oana, Smith, Adam C., Fei, Yan-Ling, Nishikawa, Joy, Stockley, Tracy L., Best, Lyle, Chitayat, David, Olney, Ann, Ives, Elizabeth, Schneider, Adele, Bestor, Timothy H., Li, Madeline, Sadowski, Paul, Squire, Jeremy

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A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundland Families (S43.002) von Meijer, Inge, Bourassa, Cynthia, Merner, Nancy, Grewal, Kanwal, Stefanelli, Mark, Hodgkinson, Kathleen, Ives, Elizabeth, Pryse-Phillips, William, Jog, Mandar, Boycott, Kym, Grimes, David, Goobie, Sharan, Leckey, Richard, Dion, Patrick, Rouleau, Guy

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1 von YOUNG, Terry-Lynn, IVES, Elizabeth, KING, Mary-Claire, LYNCH, Eric, PERSON, Richard, SNOOK, Stephanie, MACLAREN, Linda, CATOR, Tracey, GRIFFIN, Anne, FERNANDEZ, Bridget, LEE, Ming K

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Sorsby's fundus dystrophy is genetically linked to chromosome 22q13-qter von Weber, Bernhard H.F, Vogt, Gudrun, Wolz, Werner, Ives, Elizabeth J, Ewing, Cecil C

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OLDER, HYPERTENSIVE, AND HYPERCHOLESTEROLEMIC FAIRGOERS VISIT MORE BOOTHS AND DIFFER IN THEIR HEALTH CONCERNS AT A COMMUNITY HEALTH FAIR von Mess, Sarah E., Reese, Peter P., Lana, David F. Della, Walley, Alexander Y., Ives, Elizabeth P., Lee, Michael C.

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Whistle-stopping with Adlai von Dick, Jane

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Risk modifiers in carriers of brca1 mutations von Narod, Steven A., Goldgar, David, Cannon‐Albright, Lisa, Weber, Barbara, Moslehi, Roxanna, Ives, Elizabeth, Lenoir, Gilbert, Lynch, Henry

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Erratum: Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 von Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn

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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 von Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, Maclaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-claire, Young, Terry-lynn

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Science and learning in France, with a survey of opportunities for American students in French universities; an appreciation by American scholars

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Folate and vitamin B12 status of women in Newfoundland at their first prenatal visit von House, James D, March, Sandra B, Ratnam, Sam, Ives, Elizabeth, Brosnan, John T, Friel, James K

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