Mapping cutaneous field carcinogenesis of nonmelanoma skin cancer using mesoscopic imaging of pro‐inflammation cues von Shugar, Andrea L., Konger, Raymond L., Rohan, Craig A., Travers, Jeffrey B., Kim, Young L.

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The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome von Zaleski, Christina, Bassett, Anne S., Tam, Karen, Shugar, Andrea L., Chow, Eva W.C., McPherson, Elizabeth

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An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome von Shugar, Andrea L., Shapiro, Jessica M., Cytrynbaum, Cheryl, Hedges, Stephanie, Weksberg, Rosanna, Fishman, Leona

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Risk for Patient Harm in Canadian Genetic Counseling Practice: It’s Time to Consider Regulation von Shugar, Andrea L., Quercia, Nada, Trevors, Christopher, Rabideau, Marina M., Ahmed, Sohnee

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The family history: An integral component of paediatric health assessment von Shugar, Andrea L

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The mental health and traumatic experiences of mothers of children with 22q11DS von Finless, Alexandra, Rideout, Andrea L, Xiong, Ting, Carbyn, Holly, Lingley-Pottie, Patricia, Palmer, Lisa D, Shugar, Andrea, McDonald-McGinn, Donna M, McGrath, Patrick J, Bassett, Anne S, Cytrynbaum, Cheryl, Orr, Matt, Swillen, Ann, Meier, Sandra

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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation von Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.

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Analysis of elements of interlenticular opacification von Werner, Liliana, Apple, David J, Pandey, Suresh K, Solomon, Kerry D, Snyder, Michael E, Brint, Stephen F, Gayton, Johnny L, Shugar, Joel K, Trivedi, Rupal H, Izak, Andrea M

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The mental health and traumatic experiences of mothers of children with 22q11DS von Finless, Alexandra, Rideout, Andrea L, Xiong, Ting, Carbyn, Holly, Lingley-Pottie, Patricia, Palmer, Lisa D, Shugar, Andrea, McDonald-McGinn, Donna M, McGrath, Patrick J, Bassett, Anne S, Cytrynbaum, Cheryl, Orr, Matt, Swillen, Ann, Meier, Sandra

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Analysis of elements of interlenticular opacification11The authors have no financial or proprietary interest in any product mentioned in this paper von Werner, Liliana, Apple, David J, Pandey, Suresh K, Solomon, Kerry D, Snyder, Michael E, Brint, Stephen F, Gayton, Johnny L, Shugar, Joel K, Trivedi, Rupal H, Izak, Andrea M

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Dépistage des porteurs de thalassémie et d’hémoglobinopathies au Canada von Langlois, Sylvie, MD, Ford, Jason C., MD, Chitayat, David, MD, Désilets, Valérie A., MD, Farrell, Sandra A., MD, Geraghty, Michael, MD, Nelson, Tanya, PhD, Nikkel, Sarah M., MD, Skidmore, David, MD, Shugar, Andrea, MSc, Wilson, R. Douglas, MD, Johnson, Jo-Ann, MD, Audibert, François, MD, Allen, Victoria M., MD, Gagnon, Alain, MD, Blight, Claire, Wyatt, Philip R., MD

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Dépistage du X fragile en obstétrique-gynécologie au Canada von Chitayat, David, MD, Wyatt, Philip R., MD, Douglas Wilson, R, Johnson, Jo-Ann, MD, Audibert, François, MD, Allen, Victoria, MD, Gagnon, Alain, MD, Langlois, Sylvie, MD, Blight, Claire, Brock, Jo-Ann, MD, Désilets, Valérie, MD, Désilets, Valérie A., MD, Farrell, Sandra A., MD, Geraghty, Michael, MD, Nelson, Tanya, PhD, Nikkel, Sarah M., MD, Skidmore, David, MD, Shugar, Andrea, MSc

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Dépistage prénatal de l’aneuploïdie foetale von Summers, Anne M., MD, Langlois, Sylvie, MD, Wyatt, Phil, MD, PhD, Wilson, R. Douglas, MD, Allen, Victoria, MD, Blight, Claire, Désilets, Valérie, MD, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Chitayat, David, MD, Chudley, Albert E., MD, Farrell, Sandra A., MD, Geraghty, Michael T., MD, Li, Chumei, MD, PhD, Nikkel, Sarah M., MD, Shugar, Andrea, MS, Summers, Anne, MD, Tihy, Frédérique, PhD, Morin, Lucie, MD, Van den Hof, Michael, MD, Bly, Stephen, MD, Gagnon, Robert, MD, Lewthwaite, Barbara, Cargill, Yvonne M., MD, Ian Lim, Kenneth, MD, Ouellet, Annie, MD

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Archivée: Dépistage du X fragile en obstétrique-gynécologie au Canada von Chitayat, David, Wyatt, Philip R., Douglas Wilson, R., Johnson, Jo-Ann, Audibert, François, Allen, Victoria, Gagnon, Alain, Langlois, Sylvie, Blight, Claire, Brock, Jo-Ann, Désilets, Valérie, Désilets, Valérie A., Farrell, Sandra A., Geraghty, Michael, Nelson, Tanya, Nikkel, Sarah M., Skidmore, David, Shugar, Andrea

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Archivée: Dépistage prénatal de l’aneuploïdie foetale von Summers, Anne M., Langlois, Sylvie, Wyatt, Phil, Wilson, R. Douglas, Allen, Victoria, Blight, Claire, Désilets, Valérie, Gagnon, Alain, Johnson, Jo-Ann, Chitayat, David, Chudley, Albert E., Farrell, Sandra A., Geraghty, Michael T., Li, Chumei, Nikkel, Sarah M., Shugar, Andrea, Summers, Anne, Tihy, Frédérique, Morin, Lucie, Van den Hof, Michael, Bly, Stephen, Gagnon, Robert, Lewthwaite, Barbara, Cargill, Yvonne M., Ian Lim, Kenneth, Ouellet, Annie

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