Technique for determination of human zinc absorption from measurement of radioactivity in a fecal sample or the body von Payton, K B, Flanagan, P R, Stinson, E A, Chodirker, D P, Chamberlain, M J, Valberg, L S

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TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone von Huang, Lijia, Szymanska, Katarzyna, Jensen, Victor L., Janecke, Andreas R., Innes, A. Micheil, Davis, Erica E., Frosk, Patrick, Li, Chunmei, Willer, Jason R., Chodirker, Bernard N., Greenberg, Cheryl R., McLeod, D. Ross, Bernier, Francois P., Chudley, Albert E., Müller, Thomas, Shboul, Mohammad, Logan, Clare V., Loucks, Catrina M., Beaulieu, Chandree L., Bowie, Rachel V., Bell, Sandra M., Adkins, Jonathan, Zuniga, Freddi I., Ross, Kevin D., Wang, Jian, Ban, Matthew R., Becker, Christian, Nürnberg, Peter, Douglas, Stuart, Craft, Cheryl M., Akimenko, Marie-Andree, Hegele, Robert A., Ober, Carole, Utermann, Gerd, Bolz, Hanno J., Bulman, Dennis E., Katsanis, Nicholas, Blacque, Oliver E., Doherty, Dan, Parboosingh, Jillian S., Leroux, Michel R., Johnson, Colin A., Boycott, Kym M.

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Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome von Lynch, Danielle C., Revil, Timothée, Schwartzentruber, Jeremy, Bhoj, Elizabeth J., Innes, A. Micheil, Lamont, Ryan E., Lemire, Edmond G., Chodirker, Bernard N., Taylor, Juliet P., Zackai, Elaine H., McLeod, D. Ross, Kirk, Edwin P., Hoover-Fong, Julie, Fleming, Leah, Savarirayan, Ravi, Majewski, Jacek, Jerome-Majewska, Loydie A., Parboosingh, Jillian S., Bernier, Francois P.

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Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred von Houston, B.L., Zelinski, T., Israels, S.J., Coghlan, G., Chodirker, B.N., Gallagher, P.G., Houston, D.S., Zarychanski, R.

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Origin of a Prenatal Mosaic Supernumerary Neocentromeric Derivative Chromosome 13 Determined by QF-PCR von Dawson, A.J., Hryshko, M., Konkin, D., Bal, S., Bernier, D., Tomiuk, M., Burnett, S., Frosk, P., Chodirker, B.N., Chun, K.

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Clinical genetics and the Hutterite population: A review of Mendelian disorders von Boycott, Kym M., Parboosingh, Jillian S., Chodirker, Bernie N., Lowry, R. Brian, McLeod, D. Ross, Morris, Jackie, Greenberg, Cheryl R., Chudley, Albert E., Bernier, Francois P., Midgley, Julian, Møller, Lisbeth Birk, Innes, A. Micheil

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Cytogenetic microarrays in Manitoba patients with developmental delay von Dawson, AJ, Riordan, D, Tomiuk, M, Konkin, D, Anderson, T, Bocangel, P, Lwiwiski, N, Saltel-Olson, J, Marles, S, Greenberg, CR, Mhanni, A, Chodirker, BN, Chudley, AE

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Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome von Boycott, Kym M., Parboosingh, Jillian S., Scott, James N., McLeod, D. Ross, Greenberg, Cheryl R., Fujiwara, T. Mary, Mah, Jean K., Midgley, Julian, Wade, Andrew, Bernier, Francois P., Chodirker, Bernard N., Bunge, Martin, Innes, A. Micheil

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TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition von Huang, Lijia, Szymanska, Katarzyna, Jensen, Victor L, Janecke, Andreas R, Innes, A Micheil, Davis, Erica E, Frosk, Patrick, Li, Chunmei, Willer, Jason R, Chodirker, Bernard N, Greenberg, Cheryl R, McLeod, D Ross, Bernier, Francois P, Chudley, Albert E, Müller, Thomas, Shboul, Mohammad, Logan, Clare V, Loucks, Catrina M, Beaulieu, Chandree L, Bowie, Rachel V, Bell, Sandra M, Adkins, Jonathan, Zuniga, Freddi I, Ross, Kevin D, Wang, Jian, Ban, Matthew R, Becker, Christian, Nürnberg, Peter, Douglas, Stuart, Craft, Cheryl M, Akimenko, Marie-Andree, Hegele, Robert A, Ober, Carole, Utermann, Gerd, Bolz, Hanno J, Bulman, Dennis E, Katsanis, Nicholas, Blacque, Oliver E, Doherty, Dan, Parboosingh, Jillian S, Leroux, Michel R, Johnson, Colin A, Boycott, Kym M

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Reactions to alteplase in patients with acute thrombotic stroke von Chodirker, W B

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Cytogenetic microarrays in Manitoba patients with developmental delay. Authors' reply von DAWSON, A. J, RIORDAN, D, MHANNI, A, CHODIRKER, B. N, CHUDLEY, A. E, TOMIUK, M, KONKIN, D, ANDERSON, T, BOCANGEL, P, LWIWISKI, N, SALTEL-OLSON, J, MARTES, S, GREENBERG, C. R

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Bowen–Conradi syndrome: A clinical and genetic study von Lowry, R.B., Innes, A.M., Bernier, F.P., McLeod, D.R., Greenberg, C.R., Chudley, A.E., Chodirker, B., Marles, S.L., Crumley, M.J., Loredo‐Osti, J.C., Morgan, K., Fujiwara, T.M.

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Paracentric inversion 11q in Canadian Hutterites von CHODIRKER, B. N, GREENBERG, C. R, PABELLO, P. D, CHUNDLEY, A. E

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An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes von Wheway, G, Schmidts, M, Mans, DA, Szymanska, K, Nguyen, TT, Racher, H, Phelps, IG, Toedt, G, Kennedy, J, Wunderlich, KA, Sorusch, N, Abdelhamed, ZA, Natarajan, S, Herridge, W, van Reeuwijk, J, Horn, N, Boldt, K, Parry, DA, Letteboer, SJ, Roosing, S, Adams, M, Bell, SM, Bond, J, Higgins, J, Morrison, EE, Tomlinson, DC, Slaats, GG, van Dam, TJ, Huang, L, Kessler, K, Giessl, A, Logan, CV, Boyle, EA, Shendure, J, Anazi, S, Aldahmesh, M, Al Hazzaa, S, Hegele, RA, Ober, C, Frosk, P, Mhanni, AA, Chodirker, BN, Chudley, AE, Lamont, R, Bernier, FP, Beaulieu, CL, Gordon, P, Pon, RT, Donahue, C, Barkovich, AJ, Wolf, L, Toomes, C, Thiel, CT, Boycott, KM, McKibbin, M, Inglehearn, CF, UK10K Consortium, University ofWashington Center forMendelian Genomics, Stewart, F, Omran, H, Huynen, MA, Sergouniotis, PI, Alkuraya, FS, Parboosingh, JS, Innes, AM, Willoughby, CE, Giles, RH, Webster, AR, Ueffing, M, Blacque, O, Gleeson, JG, Wolfrum, U, Beales, PL, Gibson, T, Doherty, D, Mitchison, HM, Roepman, R, Johnson, CA

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Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome von Wang, Michael S., Schinzel, Albert, Kotzot, Dieter, Balmer, Damina, Casey, Robin, Chodirker, Bernie N., Gyftodimou, Jolanda, Petersen, Michael B., Lopez-Rangel, Elana, Robinson, Wendy P.

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Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16 von Chodirker, Bernard N., Ray, Manoranjan, McAlpine, Phyllis J., Riordan, Diane, Vust, Alice, Pugh, Dora, Chudley, Albert E., Opitz, John M., Reynolds, James F.

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