Isolation and characterization of epidermal growth factor from human milk von Petrides, Petro E., Hosang, Markus, Shooter, Eric, Esch, Frederic S., Böhlen, Peter

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MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome von Thues, Cedric, Valadas, Jorge S., Deaulmerie, Liesbeth, Geens, Ann, Chouhan, Amit K., Duran-Romaña, Ramon, Schymkowitz, Joost, Rousseau, Frederic, Bartusel, Michaela, Rehimi, Rizwan, Rada-Iglesias, Alvaro, Verstreken, Patrik, Van Esch, Hilde

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Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation von Froyen, Guy, Corbett, Mark, Vandewalle, Joke, Jarvela, Irma, Lawrence, Owen, Meldrum, Cliff, Bauters, Marijke, Govaerts, Karen, Vandeleur, Lucianne, Van Esch, Hilde, Chelly, Jamel, Sanlaville, Damien, van Bokhoven, Hans, Ropers, Hans-Hilger, Laumonnier, Frederic, Ranieri, Enzo, Schwartz, Charles E., Abidi, Fatima, Tarpey, Patrick S., Futreal, P. Andrew, Whibley, Annabel, Raymond, F. Lucy, Stratton, Michael R., Fryns, Jean-Pierre, Scott, Rodney, Peippo, Maarit, Sipponen, Marjatta, Partington, Michael, Mowat, David, Field, Michael, Hackett, Anna, Marynen, Peter, Turner, Gillian, Gécz, Jozef

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denommé-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gérard, Bénédicte, Mazel, Benoît, Philippe, Christophe, Pinson, Lucile, Prouteau, Clément, Putoux, Audrey, Tran Mau-Them, Frédéric, Viora-Dupont, Éléonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amélie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortüm, Fanny, Lisfeld, Jasmin, Debray, François-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, López-González, Vanesa, Kibaek, Maria, Tørring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Õunap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome von Thues, Cedric, Valadas, Jorge S, Deaulmerie, Liesbeth, Geens, Ann, Chouhan, Amit K, Duran-Romana, Ramon, Schymkowitz, Joost, Rousseau, Frederic, Bartusel, Michaela, Rehimi, Rizwan, Rada-Iglesias, Alvaro, Verstreken, Patrik, Van Esch, Hilde

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Opinion on Maintaining In-House GLP Status for Toxicologic Pathology in Pharmaceutical and (Agro)Chemical Development von Gauthier, Béatrice E., Bach, Ute, Chanut, Franck, De Jonghe, Sandra, Groeters, Sibylle, Mueller, Gundi, Palazzi, Xavier, Pohlmeyer-Esch, Gabriele, Rinke, Matthias, Schorsch, Frédéric

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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant von Aerden, Mio, Denomme-Pichon, Anne-Sophie, Bonneau, Dominique, Bruel, Ange-Line, Delanne, Julian, Gerard, Benedicte, Mazel, Benoit, Philippe, Christophe, Pinson, Lucile, Prouteau, Clement, Putoux, Audrey, Tran Mau-Them, Frederic, Viora-Dupont, Eleonore, Vitobello, Antonio, Ziegler, Alban, Piton, Amelie, Isidor, Bertrand, Francannet, Christine, Maillard, Pierre-Yves, Julia, Sophie, Philippe, Anais, Schaefer, Elise, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette, Legius, Eric, Theunis, Miel, Keren, Boris, Buratti, Julien, Charles, Perrine, Courtin, Thomas, Misra-Isrie, Mala, van Haelst, Mieke, Waisfisz, Quinten, Wieczorek, Dagmar, Schmetz, Ariane, Herget, Theresia, Kortuem, Fanny, Lisfeld, Jasmin, Debray, Francois-Guillaume, Bramswig, Nuria C, Atallah, Isis, Fodstad, Heidi, Jouret, Guillaume, Almoguera, Berta, Tahsin-Swafiri, Saoud, Santos-Simarro, Fernando, Palomares-Bralo, Maria, Lopez-Gonzalez, Vanesa, Kibaek, Maria, Torring, Pernille M, Renieri, Alessandra, Bruno, Lucia Pia, Ounap, Katrin, Wojcik, Monica, Hsieh, Tzung-Chien, Krawitz, Peter, Van Esch, Hilde

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32 Accuracy of Confocal Laser Endomicroscopy for the Diagnosis of Indeterminate Biliary Strictures: Comparison of the Miami and Paris Classifications von Sarah, Leblanc, Berson, Alain, Dhooge, Marion, Esch, Anouk, Tabouret, Tessa, Chaussade, Stanislas, Prat, Frederic

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De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas von Tolchin, Dara, Yeager, Jessica P, Prasad, Priya, Dorrani, Naghmeh, Russi, Alvaro Serrano, Martinez-Agosto, Julian A, Haseeb, Abdul, Angelozzi, Marco, Santen, G.W.E, Ruivenkamp, Claudia, Mercimek-Andrews, Saadet, Depienne, Christel, Kuechler, Alma, Mikat, Barbara, Ludecke, Hermann-Josef, Bilan, Frederic, Le Guyader, Gwenael, Gilbert-Dussardier, Brigitte, Keren, Boris, Heide, Solveig, Haye, Damien, Van Esch, Hilde, Keldermans, Liesbeth, Ortiz, Damara, Lancaster, Emily, Krantz, Ian D, Krock, Bryan L, Pechter, Kieran B, Arkader, Alexandre, Medne, Livija, DeChene, Elizabeth T, Calpena, Eduardo, Melistaccio, Giada, Wilkie, Andrew O.M, Suri, Mohnish, Foulds, Nicola, Begtrup, Amber, Henderson, Lindsay B, Forster, Cara, Reed, Patrick, McDonald, Marie T, McConkie-Rosell, Allyn, Thevenon, Julien, Le Tanno, Pauline, Coutton, Charles, Tsai, Anne C.H, Stewart, Sarah, Maver, Ales, Gorazd, Rudolf, Pichon, Olivier, Nizon, Mathilde, Cogne, Benjamin, Isidor, Bertrand, Martin-Coignard, Dominique, Stoeva, Radka, Lefebvre, Veronique, Le Caignec, Cedric

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Gastric emptying evaluation by ultrasound prior colonoscopy:An easy tool following bowel preparation von Coriat, Romain, Polin, Vanessa, Oudjit, Ammar, Henri, Franck, Dhooge, Marion, Leblanc, Sarah, Delchambre, Chantal, Esch, Anouk, Tabouret, Tessa, Barret, Maximilien, Prat, Frédéric, Chaussade, Stanislas

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Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study von Heesterbeek, Catharina J., Tjan-Heijnen, Vivianne C.G., Heimovaara, Joosje H., Lenaerts, Liesbeth, Lok, Christianne, Vriens, Ingeborg J.H., Van Opstal, Diane, Boon, Elles M.J., Sie, Daoud, de Die-Smulders, Christine E.M., Amant, Frédéric, Macville, Merryn V.E., Sistermans, E.A., Henneman, L., Polstra, A., Voorhoeve, E., Zelderen-Bohla, S.L., Boon, E.M.J., Lombardi, M.P.R., Louwerens-Zintel, C., Smit, M., van Maarle, M.C., Tan-Sindhunata, M.B., van der Meij, K., Meij, H., Bax, C., Pajkrt, E., Linskens, I.H., Martin, L., Gitsels-van der Wal, J.T., Galjaard, R.J.H., Van Opstal, D., Srebniak, M.I., Jehee, F.M. Sarquis, Hollink, I.H.I.M., Sleutels, F., de Valk, W., Deelen, W.H., Joosten, A.M.S., Diderich, K.E.M., Redeker, M.E., Go, A.T.J.I., Knapen, M.F.C.M., Galjaard, S., Prinsen, A.K.E., Braat, A.P.G., Macville, M.V.E., Stevens, S.J.C., van der Wijngaard, A., Houben, L.H., van Esch-Lennarts, M.A.A., Hamers, L., Jetten, A.G.P., Ghesquiere, S.A.I., Koning, B. de, ZamaniEsteki, M., Heesterbeek, C.J., de Die-Smulders, C.E.M., Brunner, H., Pieters, M.J., Coumans, A.B.C., Smeets, D.F.C.M., Faas, B.H.W., Westra, D., Weiss, M.M., Derks-Prinsen, I., Feenstra, I., van Rij, M., Sikkel, E., Hoffer, M.J.V., Hollander, N.S. den, Verweij, E.J.T., Haak, M.C., Suijkerbuijk, R.F., Sikkema-Raddatz, B., van Langen, I.M., Bouman, K., Duin, L.K., Schuring-Blom, G.H., Lichtenbelt, K.D., Bekker, M.N., van der Ven, A.J.E.M., van Vliet-Lachotzki, E., Pot, J., van ‘t Padje, S., Bakker, I.M.C., Bradley, E.J.

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A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation von Zanni, Ginevra, van Esch, Hilde, Bensalem, Anissa, Saillour, Yoann, Poirier, Karine, Castelnau, Laetitia, Ropers, Hans Hilger, de Brouwer, Arjan P. M., Laumonnier, Fréderic, Fryns, Jean-Pierre, Chelly, Jamel

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The expansion of endoscopic submucosal dissection in France: A prospective nationwide survey von Barret, Maximilien, Lepilliez, Vincent, Coumaros, Dimitri, Chaussade, Stanislas, Leblanc, Sarah, Ponchon, Thierry, Fumex, Fabien, Chabrun, Edouard, Bauret, Paul, Cellier, Christophe, Coron, Emmanuel, Bichard, Philippe, Bulois, Philippe, Charachon, Antoine, Rahmi, Gabriel, Bellon, Serge, Lerhun, Marc, Arpurt, Jean-Pierre, Koch, Stéphane, Napoleon, Bertrand, Vaillant, Eric, Esch, Anouk, Farhat, Said, Robin, Francoise, Kaddour, Nadira, Prat, Frédéric

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Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability von Pagan, Cecile, Botros, Hany Goubran, Poirier, Karine, Dumaine, Anne, Jamain, Stéphane, Moreno, Sarah, de Brouwer, Arjan, Van Esch, Hilde, Delorme, Richard, Launay, Jean-Marie, Tzschach, Andreas, Kalscheuer, Vera, Lacombe, Didier, Briault, Sylvain, Laumonnier, Frédéric, Raynaud, Martine, van Bon, Bregje W, Willemsen, Marjolein H, Leboyer, Marion, Chelly, Jamel, Bourgeron, Thomas

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Associative properties of perfluorooctyl end-functionalized polystyrene-poly(ethylene oxide) diblock copolymers von Boschet, Frédéric, Branger, Catherine, Margaillan, André, Hogen-Esch, Thieo E

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Discovery of a New Class of Non‐imidazole Oxazoline‐Based Histamine H 3 Receptor (H 3 R) Inverse Agonists von Célanire, Sylvain, Wijtmans, Maikel, Christophe, Bernard, Collart, Philippe, de Esch, Iwan, Dassesse, Donald, Delaunoy, Christel, Denonne, Frédéric, Durieu, Véronique, Gelens, Edith, Gillard, Michel, Lallemand, Bénédicte, Lamberty, Yves, Lebon, Florence, Nicolas, Jean‐Marie, Quéré, Luc, Snip, Erwin, Vanbellinghen, Alain, Van houtvin, Nathalie, Verbois, Valérie, Timmerman, Henk, Talaga, Patrice, Leurs, Rob, Provins, Laurent

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Complex Formation of β-Cyclodextrin- and Perfluorocarbon-Modified Water-Soluble Polymers von Zhang, Huashi, Hogen-Esch, Thieo E, Boschet, Frédéric, Margaillan, André

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Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability von Pagan, Cecile, Goubran-Botros, Hany, Poirier, Karine, Dumaine, Anne, Jamain, Stephane, Moreno, Sarah, de Brouwer, Arjan, Van Esch, Hilde, Delorme, Richard, Launay, Jean-Marie, Tzschach, Andreas, Kalscheuer, Vera M, Lacombe, Didier, Briault, Sylvain, Laumonnier, Frederic, Raynaud, Martine, van Bon, Bregje W, Willemsen, Marjolein H, Leboyer, Marion, Chelly, Jamel, Bourgeron, Thomas

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Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation von Froyen, Guy, Corbett, Mark, Vandewalle, Joke, Jarvela, Irma, Lawrence, Owen, Meldrum, Cliff, Bauters, Marijke, Govaerts, Karen, Vandeleur, Lucianne, Esch, Hilde Van, Chelly, Jamel, Saniaville, Damien, Bokhoven, Hans van, Ropers, Hans- Hilger, Laumonnier, Frederic, Ranieri, Enzo, Schwartz, Charles E, Abidi, Fatima, Tarpey, Patrick S, Futreal, P Andrew, Whibley, Annabel, Raymond, F Lucy, Stratton, Michael R, Fryns, Jean-Pierre, Scott, Rodney, Peippo, Maarit, Sipponen, Marjatta, Partington, Michael, Mowat, David, Field, Michael, Hackett, Anna, Marynen, Peter, Turner, Gillian, Gécz, Jozef

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Histamine H3 receptor ligands with a 3-cyclobutoxy motif: a novel and versatile constraint of the classical 3-propoxy linker von Wijtmans, Maikel, Denonne, Frédéric, Célanire, Sylvain, Gillard, Michel, Hulscher, Saskia, Delaunoy, Christel, Van houtvin, Nathalie, Bakker, Remko A., Defays, Sabine, Gérard, Julien, Grooters, Luc, Hubert, Delphine, Timmerman, Henk, Leurs, Rob, Talaga, Patrice, de Esch, Iwan J. P., Provins, Laurent

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