Improving care for orthopaedic patients undergoing surgery for hip fracture and total knee replacement through best practice by Bisaillon, Susan, Faraone, Jennifer, Elliott, Kathy, Cuthbert, Jane, Doucette, Cindy, Shaw, Joan

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Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene by Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, French, Curtis R., Singh, Sushma, Werdyani, Salem, Burt, Taylor, Abdelfatah, Nelly, Houston, Jim, Doucette, Lance P., Squires, Jessica, Glaser, Fabian, Roslin, Nicole M., Vincent, Daniel, Marquis, Pascale, Woodland, Geoffrey, Benoukraf, Touati, Hawkey-Noble, Alexia, Avraham, Karen B., Stanton, Susan G., Young, Terry-Lynn

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A pathogenic deletion in Forkhead Box L1 gene by Abdelfatah, Nelly, Mostafa, Ahmed A, French, Cu, Doucette, Lance P, Penney, Cindy, Lucas, Matthew B, Griffin, Anne

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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene by Abdelfatah, Nelly, Mostafa, Ahmed A., French, Curtis R., Doucette, Lance P., Penney, Cindy, Lucas, Matthew B., Griffin, Anne, Booth, Valerie, Rowley, Christopher, Besaw, Jessica E., Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Hodgkinson, Kathy A., Little, Leichelle A., Agrawal, Sumit, Parnes, Lorne, Batten, Tony, Moore, Susan, Hu, Pingzhao, Pater, Justin A., Houston, Jim, Galutira, Dante, Benteau, Tammy, MacDonald, Courtney, French, Danielle, O’Rielly, Darren D., Stanton, Susan G., Young, Terry-Lynn

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Brief Report: Impact of Reflex Testing on Tissue-Based Molecular Genotyping in Patients With Advanced Non-Squamous Non-Small Cell Lung Cancer by Marmarelis, Melina E, Scholes, Dylan G, McGrath, Cindy M, Priore, Salvatore F, Roth, Jacquelyn J, Feldman, Michael, Morrissette, Jennifer J D, Litzky, Leslie, Deshpande, Charu, Thompson, Jeffrey C, Doucette, Abigail, Gabriel, Peter E, Sun, Lova, Singh, Aditi P, Cohen, Roger B, Langer, Corey J, Carpenter, Erica L, Aggarwal, Charu

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Cytokine Profiles of Severe Influenza Virus-Related Complications in Children by Fiore-Gartland, Andrew, Panoskaltsis-Mortari, Angela, Agan, Anna A, Mistry, Anushay J, Thomas, Paul G, Matthay, Michael A, Hertz, Tomer, Randolph, Adrienne G

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Staphylococcus aureus α-Toxin Response Distinguishes Respiratory Virus–Methicillin-Resistant S. aureus Coinfection in Children by Yu, Karl O. A., Randolph, Adrienne G., Agan, Anna A., Yip, Wai-Ki, Truemper, Edward J., Weiss, Scott L., Ackerman, Kate G., Schwarz, Adam J., Giuliano, John S., Hall, Mark W., Wardenburg, Juliane Bubeck

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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 by 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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Validation of the APTIMA Combo 2 Assay for the Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in SurePath Liquid-Based Pap Test Samples Taken With Different Collectio... by Chernesky, Max, Jang, Dan, Smieja, Marek, Portillo, Eder, Ewert, Ruth, Pritchard, Cindy, MacEachern, Diane, Doucette, Christine, MacDonald, Anne, Kapala, Julius, Sumner, Jeff, Hill, Craig

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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 by 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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