Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus von Kuentz, P., Fraitag, S., Gonzales, M., Dhombres, F., St‐Onge, J., Duffourd, Y., Joyé, N., Jouannic, J.‐M., Picard, A., Marle, N., Thevenon, J., Thauvin‐Robinet, C., Faivre, L., Rivière, J.‐B., Vabres, P.

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Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses von Vialard, F, Ottolenghi, C, Gonzales, M, Choiset, A, Girard, S, Siffroi, J P, McElreavey, K, Vibert-Guigue, C, Sebaoun, M, Joyé, N, Portnoï, M F, Jaubert, F, Fellous, M

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Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development von Sanlaville, D, Etchevers, H C, Gonzales, M, Martinovic, J, Clément-Ziza, M, Delezoide, A-L, Aubry, M-C, Pelet, A, Chemouny, S, Cruaud, C, Audollent, S, Esculpavit, C, Goudefroye, G, Ozilou, C, Fredouille, C, Joye, N, Morichon-Delvallez, N, Dumez, Y, Weissenbach, J, Munnich, A, Amiel, J, Encha-Razavi, F, Lyonnet, S, Vekemans, M, Attié-Bitach, T

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Role of chromosome abnormalities in ectopic pregnancy von Coste, Joël, Fernandez, Hervé, Joyé, Nicole, Benifla, Jean-Louis, Girard, Sylvie, Marpeau, Loı̈c, Job-Spira, Nadine

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Discontinuous gradient centrifugation (DGC) decreases the proportion of chromosomally unbalanced spermatozoa in chromosomal rearrangement carriers von Rouen, Alexandre, Balet, Richard, Dorna, Maud, Hyon, Capucine, Pollet-Villard, Xavier, Chantot-Bastaraud, Sandra, Joyé, Nicole, Portnoï, Marie-France, Cassuto, Nino Guy, Siffroi, Jean-Pierre

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Prenatal detection of Pierre Robin sequence with deletion Xp and additional trisomy 14q by telomere screening von Gerard-Blanluet, M., Pipiras, E., Levaillant, J. M., Joye, N., Koubi, V., Kanafani, S., Vergnaud, A., Verloes, A., Gonzales, M., Jeny, R., Benzacken, B.

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Children's anticipation of and response to colposcopic examination von Steward, Margaret S., Schmitz, Martha, Steward, David S., Joye, Nancy R., Reinhart, Michael

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Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly von Benzacken, B, Siffroi, J P, Le Bourhis, C, Krabchi, K, Joyé, N, Maschino, F, Viguié, F, Soulié, J, Gonzales, M, Migné, G, Bucourt, M, Encha-Razavi, F, Carbillon, L, Taillemite, J L

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Un panel français: L’Étude longitudinale par Internet pour les sciences sociales (Elipss) von Duwez, Emmanuelle, Mercklé, Pierre

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Prenatal diagnosis by FISH of a 22q11 deletion in two families von Portnoï, M F, Joyé, N, Gonzales, M, Demczuk, S, Fermont, L, Gaillard, G, Bercau, G, Morlier, G, Taillemite, J L

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Ving-cinq ans après: Les femmes au rendez-vous de l’histoire

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French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature von Luquet, I, Mugneret, F, Athis, P.D, Nadal, N, Favre, B, Abel, C, Chelloug, N, Lespinasse, J, Portnoi, M.F, Joyé, N, Dupont, J.M, Lebbar, A, Bresson, J.L, Fellmann, F, Siffroi, J.P, Chantot-Bastaraud, S, Chiesa, J, Amblard, F, Devillard, F, Jeandidier, E, Boceno, M, Rival, J.M, Bellec, V, Lallaoui, H, Delobel, B, Croquette, M.F, Benzacken, B

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Capturing the Nature of the Spelling Errors in Developmental Language Disorder: A Scoping Review von Broc, L, Joye, N, Dockrell, JE, Olive, T

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Diaphanospondylodysostosis (DSD): Confirmation of a recessive disorder with abnormal vertebral ossification and nephroblastomatosis von Gonzales, Marie, Verloes, Alain, Frison, Marie‐Hélène Saint, Perrotez, Chantal, Bourdet, Odile, Encha‐Razavi, Ferechte, Joyé, Nicole, Taillemite, Jean‐Louis, Walbaum, Roland, Pfeiffer, Rudolf, Maroteaux, Pierre

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The Spelling Errors of French and English Children With Developmental Language Disorder at the End of Primary School von Joye, N, Dockrell, JE, Marshall, CR

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Do children with reading difficulties benefit from instructional game supports? Exploring children’s attention and understanding of feedback von Vasalou, A, Benton, L, Sumner, E, Ibrahim, S, Herbert, E, Joye, N

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Comparing the Health Status of Low-Income Children in and out of Foster Care von Hansen, Robin L., Mawjee, Fatema Lakhani, Barton, Keith, Metcalf, Mary B., Joye, Nancy R.

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Mosaic-activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus von Kuentz, P, Fraitag, S, Gonzales, M, Dhombres, F, St-Onge, J, Duffourd, Y, Joyé, N, Jouannic, J-M, Picard, A, Marle, N, Thevenon, J, Thauvin-Robinet, C, Faivre, L, Rivière, J-B, Vabres, P

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Spelling Performance in Children with Developmental Language Disorder: A Meta-Analysis across European Languages von Joye, N, Broc, L, Olive, T, Dockrell, JE

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Designing for “challenge” in a large-scale adaptive literacy game for primary school children von Benton, L, Mavrikis, M, Vasalou, A, Joye, N, Sumner, E, Herbert, E, Revesz, A, Symvonis, A, Raftopoulou, C

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