Effect of ultrasound on the induction time and the metastable zone widths of potassium sulphate von Lyczko, Nathalie, Espitalier, Fabienne, Louisnard, Olivier, Schwartzentruber, Jacques

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Extension of UNIFAC to high pressures and temperatures by the use of a cubic equation of state von Schwartzentruber, Jacques, Renon, Henri

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Influence of ultrasound power on the alkylation of phenylacetonitrile under solid-liquid phase transfer catalysis conditions von Guilet, Richard, Berlan, Jacques, Louisnard, Olivier, Schwartzentruber, Jacques

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Nucleation Control in Precipitation Processes by Ultrasound von Gatumel, Cendrine, Espitalier, Fabienne, Schwartzentruber, Jacques, Biscans, Beatrice, Wilhelm, A.M.

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Equations of state: how to reconcile flexible mixing rules, the virial coefficient constraint and the “michelsen-Kistenmacher syndrome” for multicomponent systems von Schwartzentruber, Jacques, Renon, Henri

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Dissolution of quartz into dilute alkaline solutions at 90°C: A kinetic study von Schwartzentruber, Jacques, Fürst, Walter, Renon, H.

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Protein precipitation by caprylic acid: Equilibrium composition data von Bernard, Nadine, Jolivalt, Claude, Schwartzentruber, Jacques

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Modeling of multiphase liquid equilibria for multicomponent mixtures von García-Sánchez, Fernando, Schwartzentruber, Jacques, Ammar, Mohamed N, Renon, Henri

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Development of a new cubic equation of state for phase equilibrium calculations von Schwartzentruber, Jacques, Renon, Henri, Watanasiri, Suphat

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Representation of the vapor-liquid equilibrium of the ternary system carbon dioxide - propane - methanol and its binaries with a cubic equation of state : a new mixing rule von Schwartzentruber, Jacques, Galivel-Solastiouk, Francine, Renon, Henri

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Prediction of the binary parameters of a cubic equation of state from a group-contribution method von Schwartzentruber, Jacques, Ponce-Ramirez, Luis, Renon, Henri

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Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population von Srour, Myriam, Schwartzentruber, Jeremy, Hamdan, Fadi F., Ospina, Luis H., Patry, Lysanne, Labuda, Damian, Massicotte, Christine, Dobrzeniecka, Sylvia, Capo-Chichi, José-Mario, Papillon-Cavanagh, Simon, Samuels, Mark E., Boycott, Kym M., Shevell, Michael I., Laframboise, Rachel, Désilets, Valérie, Maranda, Bruno, Rouleau, Guy A., Majewski, Jacek, Michaud, Jacques L.

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Haploinsufficiency of SF3B4, a Component of the Pre-mRNA Spliceosomal Complex, Causes Nager Syndrome von Bernier, Francois P., Caluseriu, Oana, Ng, Sarah, Schwartzentruber, Jeremy, Buckingham, Kati J., Innes, A. Micheil, Jabs, Ethylin Wang, Innis, Jeffrey W., Schuette, Jane L., Gorski, Jerome L., Byers, Peter H., Andelfinger, Gregor, Siu, Victoria, Lauzon, Julie, Fernandez, Bridget A., McMillin, Margaret, Scott, Richard H., Racher, Hilary, Majewski, Jacek, Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael J., Parboosingh, Jillian S.

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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes von Rivière, Jean-Baptiste, Mirzaa, Ghayda M, O'Roak, Brian J, Beddaoui, Margaret, Alcantara, Diana, Conway, Robert L, St-Onge, Judith, Schwartzentruber, Jeremy A, Gripp, Karen W, Nikkel, Sarah M, Worthylake, Thea, Sullivan, Christopher T, Ward, Thomas R, Butler, Hailly E, Kramer, Nancy A, Albrecht, Beate, Armour, Christine M, Armstrong, Linlea, Caluseriu, Oana, Cytrynbaum, Cheryl, Drolet, Beth A, Innes, A Micheil, Lauzon, Julie L, Lin, Angela E, Mancini, Grazia M S, Meschino, Wendy S, Reggin, James D, Saggar, Anand K, Lerman-Sagie, Tally, Uyanik, Gökhan, Weksberg, Rosanna, Zirn, Birgit, Beaulieu, Chandree L, Majewski, Jacek, Bulman, Dennis E, O'Driscoll, Mark, Shendure, Jay, Graham, John M, Boycott, Kym M, Dobyns, William B

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Mutations in NOTCH2 in families with Hajdu-Cheney syndrome von Majewski, Jacek, Schwartzentruber, Jeremy A., Caqueret, Aurore, Patry, Lysanne, Marcadier, Janet, Fryns, Jean-Pierre, Boycott, Kym M., Ste-Marie, Louis-Georges, McKiernan, Fergus E., Marik, Ivo, Van Esch, Hilde, Michaud, Jacques L., Samuels, Mark E.

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Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 von Srour, Myriam, Hamdan, Fadi F., McKnight, Dianalee, Davis, Erica, Mandel, Hanna, Schwartzentruber, Jeremy, Martin, Brissa, Patry, Lysanne, Nassif, Christina, Dionne-Laporte, Alexandre, Ospina, Luis H., Lemyre, Emmanuelle, Massicotte, Christine, Laframboise, Rachel, Maranda, Bruno, Labuda, Damian, Décarie, Jean-Claude, Rypens, Françoise, Goldsher, Dorith, Fallet-Bianco, Catherine, Soucy, Jean-François, Laberge, Anne-Marie, Maftei, Catalina, Boycott, Kym, Brais, Bernard, Boucher, Renée-Myriam, Rouleau, Guy A., Katsanis, Nicholas, Majewski, Jacek, Elpeleg, Orly, Kukolich, Mary K., Shalev, Stavit, Michaud, Jacques L.

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Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency von Berryer, Martin H., Hamdan, Fadi F., Klitten, Laura L., Møller, Rikke S., Carmant, Lionel, Schwartzentruber, Jeremy, Patry, Lysanne, Dobrzeniecka, Sylvia, Rochefort, Daniel, Neugnot-Cerioli, Mathilde, Lacaille, Jean-Claude, Niu, Zhiyv, Eng, Christine M., Yang, Yaping, Palardy, Sylvain, Belhumeur, Céline, Rouleau, Guy A., Tommerup, Niels, Immken, LaDonna, Beauchamp, Miriam H., Patel, Gayle Simpson, Majewski, Jacek, Tarnopolsky, Mark A., Scheffzek, Klaus, Hjalgrim, Helle, Michaud, Jacques L., Di Cristo, Graziella

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Mutations in TMEM231 cause Joubert syndrome in French Canadians von Srour, Myriam, Hamdan, Fadi F, Schwartzentruber, Jeremy A, Patry, Lysanne, Ospina, Luis H, Shevell, Michael I, Désilets, Valérie, Dobrzeniecka, Sylvia, Mathonnet, Géraldine, Lemyre, Emmanuelle, Massicotte, Christine, Labuda, Damian, Amrom, Dina, Andermann, Eva, Sébire, Guillaume, Maranda, Bruno, Consortium, FORGE Canada, Rouleau, Guy A, Majewski, Jacek, Michaud, Jacques L

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Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly Is Caused by a Duplication in RUNX2 von Moffatt, Pierre, Ben Amor, Mouna, Glorieux, Francis H., Roschger, Paul, Klaushofer, Klaus, Schwartzentruber, Jeremy A., Paterson, Andrew D., Hu, Pingzhao, Marshall, Christian, Fahiminiya, Somayyeh, Majewski, Jacek, Beaulieu, Chandree L., Boycott, Kym M., Rauch, Frank

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Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafne... von Schwartzentruber, Jeremy, Buhas, Daniela, Majewski, Jacek, Sasarman, Florin, Papillon-Cavanagh, Simon, Thiffaut, Isabelle, Sheldon, Katherine M., Massicotte, Christine, Patry, Lysanne, Simon, Mariella, Zare, Amir S., McKernan, Kevin J., Michaud, Jacques, Boles, Richard G., Deal, Cheri L., Desilets, Valerie, Shoubridge, Eric A., Samuels, Mark E.

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