Sexual dimorphism in white campion: complex control of carpel number is revealed by Y chromosome deletions von Lardon, A. (CNRS/INRA/ENS, Lyon, France.), Georgiev, S, Aghmir, A, Le Merrer, G, Negrutiu, I

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Calibration of quasi-static aberrations in exoplanet direct-imaging instruments with a Zernike phase-mask sensor: III. On-sky validation in VLT/SPHERE von Vigan, A., N’Diaye, M., Dohlen, K., Sauvage, J.-F., Milli, J., Zins, G., Petit, C., Wahhaj, Z., Cantalloube, F., Caillat, A., Costille, A., Le Merrer, J., Carlotti, A., Beuzit, J.-L., Mouillet, D.

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Viscous mechanism for Leidenfrost propulsion on a ratchet von Dupeux, G, Le Merrer, M, Lagubeau, G, Clanet, C, Hardt, S, Quéré, D

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Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Can Be Caused by Mutations in Either ENPP1 or ABCC6 von Nitschke, Yvonne, Baujat, Geneviève, Botschen, Ulrike, Wittkampf, Tanja, du Moulin, Marcel, Stella, Jacqueline, Le Merrer, Martine, Guest, Geneviève, Lambot, Karen, Tazarourte-Pinturier, Marie-Frederique, Chassaing, Nicolas, Roche, Olivier, Feenstra, Ilse, Loechner, Karen, Deshpande, Charu, Garber, Samuel J., Chikarmane, Rashmi, Steinmann, Beat, Shahinyan, Tatevik, Martorell, Loreto, Davies, Justin, Smith, Wendy E., Kahler, Stephen G., McCulloch, Mignon, Wraige, Elizabeth, Loidi, Lourdes, Höhne, Wolfgang, Martin, Ludovic, Hadj-Rabia, Smaïl, Terkeltaub, Robert, Rutsch, Frank

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First light of VLT/HiRISE: High-resolution spectroscopy of young giant exoplanets von Vigan, A., El Morsy, M., Lopez, M., Otten, G. P. P. L., Garcia, J., Costes, J., Muslimov, E., Viret, A., Charles, Y., Zins, G., Murray, G., Costille, A., Paufique, J., Seemann, U., Houllé, M., Anwand-Heerwart, H., Phillips, M., Abinanti, A., Balard, P., Baraffe, I., Benedetti, J.-A., Blanchard, P., Blanco, L., Beuzit, J.-L., Choquet, E., Cristofari, P., Desidera, S., Dohlen, K., Dorn, R., Ely, T., Fuenteseca, E., Garcia, N., Jaquet, M., Jaubert, F., Kasper, M., Le Merrer, J., Maire, A.-L., N’Diaye, M., Pallanca, L., Popovic, D., Pourcelot, R., Reiners, A., Rochat, S., Sehim, C., Schmutzer, R., Smette, A., Tchoubaklian, N., Tomlinson, P., Valenzuela Soto, J.

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The FAZIA setup: A review on the electronics and the mechanical mounting von Valdré, S., Casini, G., Le Neindre, N., Bini, M., Boiano, A., Borderie, B., Edelbruck, P., Poggi, G., Salomon, F., Tortone, G., Alba, R., Barlini, S., Bonnet, E., Bougard, B., Bougault, R., Brulin, G., Bruno, M., Buccola, A., Camaiani, A., Chbihi, A., Ciampi, C., Cicerchia, M., Cinausero, M., Dell’Aquila, D., Desrues, P., Dueñas, J.A., Fabris, D., Falorsi, M., Frankland, J.D., Frosin, C., Galichet, E., Giordano, R., Gramegna, F., Grassi, L., Gruyer, D., Guerzoni, M., Henri, M., Kajetanowicz, M., Korcyl, K., Kordyasz, A., Kozik, T., Lecomte, P., Lombardo, I., Lopez, O., Maiolino, C., Mantovani, G., Marchi, T., Margotti, A., Merrer, Y., Morelli, L., Olmi, A., Ordine, A., Ottanelli, P., Pain, C., Pałka, M., Pârlog, M., Pasquali, G., Pastore, G., Piantelli, S., de Préaumont, H., Revenko, R., Richard, A., Rivet, M.F., Ropert, J., Rosato, E., Saillant, F., Santonocito, D., Scarlini, E., Serra, S., Soulet, C., Spadaccini, G., Stefanini, A.A., Tobia, G., Upadhyaya, S., Vanzanella, A., Verde, G., Vient, E., Vigilante, M., Wanlin, E., Wittwer, G., Zucchini, A.

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In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome von Faivre, L, Gorlin, R J, Wirtz, M K, Godfrey, M, Dagoneau, N, Samples, J R, Le Merrer, M, Collod-Beroud, G, Boileau, C, Munnich, A, Cormier-Daire, V

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ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation von Cormier-Daire, Valérie, Le Goff, Carine, Wang, Lauren W, Ge, Gaoxiang, Bauer, Florence, Krakow, Deborah, Perrot, Claire, Flori, Elisabeth, Prost-Squarcioni, Catherine, Bonnet, Damien, Munnich, Arnold, Apte, Suneel S, Greenspan, Daniel S, Le Merrer, Martine, Dagoneau, Nathalie, Crow, Yanick J, Morice-Picard, Fanny

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Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis von Rossi, Massimiliano, Hall, Christine M., Bouvier, Raymonde, Collardeau-Frachon, Sophie, Le Breton, Frédérique, Bucourt, Martine, Cordier, Marie Pierre, Vianey-Saban, Christine, Parenti, Giancarlo, Andria, Generoso, Le Merrer, Martine, Edery, Patrick, Offiah, Amaka C.

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Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients von Flechtner, I, Lambot-Juhan, K, Teissier, R, Colmenares, A, Baujat, G, Beltrand, J, Ajaltouni, Z, Pauwels, C, Pinto, G, Samara-Boustani, D, Simon, A, Thalassinos, C, Le Merrer, M, Cormier-Daire, V, Polak, M

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Cantú Syndrome Is Caused by Mutations in ABCC9 von van Bon, Bregje W.M., Gilissen, Christian, Grange, Dorothy K., Hennekam, Raoul C.M., Kayserili, Hülya, Engels, Hartmut, Reutter, Heiko, Ostergaard, John R., Morava, Eva, Tsiakas, Konstantinos, Isidor, Bertrand, Le Merrer, Martine, Eser, Metin, Wieskamp, Nienke, de Vries, Petra, Steehouwer, Marloes, Veltman, Joris A., Robertson, Stephen P., Brunner, Han G., de Vries, Bert B.A., Hoischen, Alexander

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Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome von Baujat, Geneviève, Rio, Marlène, Rossignol, Sylvie, Sanlaville, Damien, Lyonnet, Stanislas, Le Merrer, Martine, Munnich, Arnold, Gicquel, Christine, Cormier-Daire, Valérie, Colleaux, Laurence

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Calibration of quasi-static aberrations in exoplanet direct-imaging instruments with a Zernike phase-mask sensor: II. Concept validation with ZELDA on VLT/SPHERE von N'diaye, M, Vigan, A, Dohlen, K, Sauvage, J-F, Caillat, A, Costille, A, Girard, J H V, Beuzit, J-L, Fusco, T, Blanchard, P

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Calibration of quasi-static aberrations in exoplanet direct-imaging instruments with a Zernike phase-mask sensor: IV. Temporal stability of non-common path aberrations in VLT/SPHER... von Vigan, A., Dohlen, K., N’Diaye, M., Cantalloube, F., Girard, J. H., Milli, J., Sauvage, J.-F., Wahhaj, Z., Zins, G., Beuzit, J.-L., Caillat, A., Costille, A., Le Merrer, J., Mouillet, D., Tourenq, S.

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Three‐dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasia von Macé, G., Sonigo, P., Cormier‐Daire, V., Aubry, M.‐C., Martinovic, J., Elie, C., Gonzales, M., Carbonne, B., Dumez, Y., Le Merrer, M., Brunelle, F., Benachi, A.

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Calibration of quasi-static aberrations in exoplanet direct-imaging instruments with a Zernike phase-mask sensor von Vigan, A., N’Diaye, M., Dohlen, K., Sauvage, J.-F., Milli, J., Zins, G., Petit, C., Wahhaj, Z., Cantalloube, F., Caillat, A., Costille, A., Le Merrer, J., Carlotti, A., Beuzit, J.-L., Mouillet, D.

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Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia von Huber, Céline, Faqeih, Eissa Ali, Bartholdi, Deborah, Bole-Feysot, Christine, Borochowitz, Zvi, Cavalcanti, Denise P., Frigo, Amandine, Nitschke, Patrick, Roume, Joelle, Santos, Heloísa G., Shalev, Stavit A., Superti-Furga, Andrea, Delezoide, Anne-Lise, Le Merrer, Martine, Munnich, Arnold, Cormier-Daire, Valérie

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SHOX mutations in dyschondrosteosis (Leri-Weill syndrome) von Cusin, Veronica, Viot, Géraldine, Munnich, Arnold, Toutain, Annick, Vekemans, Michel, Merrer, Martine Le, Girlich, Delphine, Cormier-Daire, Valérie, Belin, Valérie, Moncla, Anne

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Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families von Willems, M, Geneviève, D, Borck, G, Baumann, C, Baujat, G, Bieth, E, Edery, P, Farra, C, Gerard, M, Héron, D, Leheup, B, Le Merrer, M, Lyonnet, S, Martin-Coignard, D, Mathieu, M, Thauvin-Robinet, C, Verloes, A, Colleaux, L, Munnich, A, Cormier-Daire, V

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Effects of deletion of gria1 or gria2 genes encoding glutamatergic AMPA-receptor subunits on place preference conditioning in mice von Mead, Andy N, Brown, Geraldine, Le Merrer, Julie, Stephens, David N

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