Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis von Boissel, Sarah, Fallet-Bianco, Catherine, Chitayat, David, Kremer, Valérie, Nassif, Christina, Rypens, Françoise, Delrue, Marie-Ange, Dal Soglio, Dorothée, Oligny, Luc L., Patey, Natalie, Flori, Elisabeth, Cloutier, Mireille, Dyment, David, Campeau, Philippe, Karalis, Aspasia, Nizard, Sonia, Fraser, William D., Audibert, François, Lemyre, Emmanuelle, Rouleau, Guy A., Hamdan, Fadi F., Kibar, Zoha, Michaud, Jacques L.

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Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype von Szafranski, Przemyslaw, Liu, Qian, Karolak, Justyna A., Song, Xiaofei, de Leeuw, Nicole, Faas, Brigitte, Gerychova, Romana, Janku, Petr, Jezova, Marta, Valaskova, Iveta, Gibbs, Kathleen A., Surrey, Lea F., Poisson, Virginie, Bérubé, Denis, Oligny, Luc L., Michaud, Jacques L., Popek, Edwina, Stankiewicz, Paweł

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Workload Measurement in Subspecialty Placental Pathology in Canada von Wright, James R., Chan, Suzanne, Morgen, Eric K., Maung, Raymond T. A., Brundler, Marie-Anne, El Demellawy, Dina, Fraser, Robert B., Kurek, Kyle C., Magee, Fergall, Nizalik, Elizabeth, Oligny, Luc L., Somers, Gino R., Stefanovici, Camelia, Terry, Jefferson

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Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study von Razmpoosh, Maryam, Sansregret, Andrée, Oligny, Luc L, Patey, Natalie, Dormoy-Raclet, Virginie, Ducruet, Thierry, Bouron-Dal Soglio, Dorothée

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High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma von Sartelet, Hervé, Ohta, Shigeru, Barrette, Stephane, Rougemont, Anne-Laure, Brevet, Marie, Regairaz, Marie, Harvey, Isabelle, Bernard, Chantal, Fabre, Monique, Gaboury, Louis, Oligny, Luc L, Bosq, Jacques, Valteau-Couanet, Dominique, Vassal, Gilles

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Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene von Maquet, Emilie, Costagliola, Sabine, Parma, Jasmine, Christophe-Hobertus, Christiane, Oligny, Luc L., Fournet, Jean-Christophe, Robitaille, Yves, Vuissoz, Jean-Marc, Payot, Antoine, Laberge, Sophie, Vassart, Gilbert, Van Vliet, Guy, Deladoëy, Johnny

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Cardiac pathology in sudden unexpected infant death von Dancea, Adrian, Côté, Aurore, Rohlicek, Charles, Bernard, Chantal, Oligny, Luc L.

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Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis von Boissel, Sarah, Fallet-Bianco, Catherine, Chitayat, David, Kremer, Valérie, Nassif, Christina, Rypens, Françoise, Delrue, Marie-Ange, Soglio, Dorothée Dal, Oligny, Luc L, Patey, Natalie, Flori, Elisabeth, Cloutier, Mireille, Dyment, David, Campeau, Philippe, Karalis, Aspasia, Nizard, Sonia, Fraser, William D, Audibert, François, Lemyre, Emmanuelle, Rouleau, Guy A, Hamdan, Fadi F, Kibar, Zoha, Michaud, Jacques L

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Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13 von Nardi, Nicolas, Proulx, François, Brunel-Guiton, Catherine, Oligny, Luc L., Piché, Nelson, Mitchell, Grant A., Joyal, Jean Sébastien

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Pediatric Anogenital Warts: A 7-Year Review of Children Referred to a Tertiary-Care Hospital in Montreal, Canada von Marcoux, Danielle, Nadeau, Karine, McCuaig, Catherine, Powell, Julie, Oligny, Luc L.

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Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood von Battista, Marie-Claude, Oligny, Luc L, St-Louis, Jean, Brochu, Michele

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Sudden death in growth hormone–treated children with Prader-Willi syndrome von Vliet, Guy Van, Deal, Cheri L., Crock, Patricia A., Robitaille, Yves, Oligny, Luc L.

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A Two-Tier Polymerase Chain Reaction Direct Sequencing Method for Detecting and Typing Human Papillomaviruses in Pathological Specimens von Feoli-Fonseca, Juan Carlos, Filion, Mario, Brochu, Pierre, Simard, Pierre, Luc, L Oligny, Pierre, A Russo, Wagner, V Yotov

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Searching for an intrinsic neuroendocrine cell in the kidney von Guy, Laurent, R. Bégin, Louis, L. Oligny, Luc, B. Brock, Gerald, Chevalier, Simone, G. Aprikian, Armen

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Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies von Mircescu, Hortensia, Parma, Jasmine, Huot, Céline, Deal, Cheri, Oligny, Luc L., Vassart, Gilbert, Van Vliet, Guy

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Unilobar congenital pulmonary lymphangiectasis mimicking congenital lobar emphysema: an underestimated presentation? von Chapdelaine, Joyaube, Beaunoyer, Mona, St-Vil, Dickens, Oligny, Luc L., Garel, Laurent, Bütter, Andreana, Di Lorenzo, Maria

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Intrahepatic Biliary Cysts Presenting before Hepatic Portoenterostomy in Biliary Atresia von Mas, Emmanuel, Alvarez, Fernando, Oligny, Luc L., Martin, Steven

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Accessory Liver Lobe with Mesothelial Inclusion Cysts in an Omphalocele: A New Malformative Association von Rougemont, Anne-Laure, Sartelet, Hervé, Oligny, Luc L., Bensoussan, Arie, Yazbeck, Salam, Fournet, Jean-Christophe

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Basal cells of second trimester fetal breasts: immunohistochemical study of myoepithelial precursors von Jolicoeur, Francine, Gaboury, Louis A, Oligny, Luc L

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Human papillomavirus (HPV) study of 691 pathological specimens from Quebec by PCR-direct sequencing approach von Feoli-Fonseca, Juan Carlos, Oligny, Luc L., Brochu, Pierre, Simard, Pierre, Falconi, Sarah, Yotov, Wagner V.

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