GPS-tracking and colony observations reveal variation in offshore habitat use and foraging ecology of breeding Sandwich Terns von Fijn, R.C., de Jong, J., Courtens, W., Verstraete, H., Stienen, E.W.M., Poot, M.J.M.

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Faecal samples reveal the diet of breeding adult Sandwich terns Thalasseus sandvicensis in Belgium and the southern part of the Netherlands von Courtens, W., Verstraete, H., Vanermen, N., Van de walle, M., Stienen, E.W.M.

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The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene von Hoornaert, K P, Dewinter, C, Vereecke, I, Beemer, F A, Courtens, W, Fryer, A, Fryssira, H, Lees, M, Müllner-Eidenböck, A, Rimoin, D L, Siderius, L, Superti-Furga, A, Temple, K, Willems, P J, Zankl, A, Zweier, C, De Paepe, A, Coucke, P, Mortier, G R

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FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions von D'haene, B, Nevado, J, Pugeat, M, Pierquin, G, Lowry, R.B, Reardon, W, Delicado, A, García-Miñaur, S, Palomares, M, Courtens, W, Stefanova, M, Wallace, S, Watkins, W, Shelling, A.N, Wieczorek, D, Veitia, R.A, De Paepe, A, Lapunzina, P, De Baere, E

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Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics von Rooms, L, Reyniers, E, Wuyts, W, Storm, K, Van Luijk, R, Scheers, S, Wauters, J, Van Den Ende, J, Biervliet, M, Eyskens, F, Van Goethem, G, Laridon, A, Ceulemans, B, Courtens, W, Kooy, RF

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Beach nourishment: an ecologically sound coastal defence alternative? A review von Speybroeck, Jeroen, Bonte, Dries, Courtens, Wouter, Gheskiere, Tom, Grootaert, Patrick, Maelfait, Jean-Pierre, Mathys, Mieke, Provoost, Sam, Sabbe, Koen, Stienen, Eric W.M., Lancker, Vera Van, Vincx, Magda, Degraer, Steven

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Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7) von Courtens, W., Vroman, S., Vandenhove, J., Wiedemann, U., Schinzel, A.

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Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritance von Courtens, W, Johansson, A-B, Dachy, B, Avni, F, Telerman-Toppet, N, Scheffer, H

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Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation von DE BAERE, Elfride, DIXON, Michael J, COURTENS, Winnie, HJALGRIM, Helle, SHANGZHI HUANG, LIEBAERS, Inge, VAN REGEMORTER, Nicole, TOURAINE, Philippe, PRAPHANPHOJ, Verayuth, VERLOES, Alain, UDAR, Nitin, YELLORE, Vivek, SMALL, Kent W, CHALUKYA, Meenal, YELCHITS, Svetlana, DE PAEPE, Anne, KUTTENN, Frédérique, FELLOUS, Marc, VEITIA, Reiner, MESSIAEN, Ludwine, JABS, Ethylin W, LEROY, Bart P, DEVRIENDT, Koenraad, GILLEROT, Yves, MORTIER, Geert, MEIRE, Francoise, VAN MALDERGEM, Lionel

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Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion von COURTENS, W, GROSSMAN, D, SPELEMAN, F, VAN ROY, N, MESSIAEN, L, VAMOS, E, TOPPET, V, HAUMONT, D, STREYDIO, C, JAUCH, A, VERMEESCH, J. R

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A subterminal deletion of the long arm of chromosome 10: A clinical report and review von Courtens, Winnie, Wuyts, Wim, Rooms, Liesbeth, Pera, Sarah Barbera, Wauters, Jan

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Moebius syndrome in an infant exposed in utero to benzodiazepines von Courtens, W., Vamos, E., Hainaut, M., Vergauwen, P.

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Atypical Features in Angelman Syndrome Due to Imprinting Defect or Uniparental Disomy of Chromosome 15 von Dan, B., Boyd, S. G., Christiaens, Florence, Courtens, Winnie, Van Maldergem, L., Kahn, A.

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Response to "Letter: Fibular Aplasia, Tibial Campomelia and Oligosyndactyly" by Evans and Elliott von Courtens, Winnie, Vanhoenacker, Filip

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Fibular aplasia, tibial campomelia, and oligosyndactyly in a male newborn infant: A case report and review of the literature von Courtens, Winnie, Jespers, Ann, Harrewijn, Inge, Puylaert, Dirk, Vanhoenacker, Filip

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Hermansky-Pudlak syndrome : A case report and discussion von VANHOOTEGHEM, O, COURTENS, W, ANDRE, J, SASS, U, SONG, M

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Hypoparathyroidism‐retardation‐dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation—clinical report and review von Courtens, Winnie, Wuyts, Wim, Poot, Martin, Szuhai, Karoly, Wauters, Jan, Reyniers, Edwin, Eleveld, Marc, Diaz, George, Nöthen, Markus M., Parvari, Ruti

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Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiency von COHEN, L. H. F, VAMOS, E, HEINRICHS, C, TOPPET, M, COURTENS, W, KUMPS, A, MARDENS, Y, CARLSSON, B, GRILLNER, L, LARSSON, A

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New syndrome or severe expression of Gordon syndrome? A case report von Courtens, W, Perlmutter, N, Dan, B, Vamos, E

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A probable case of Wiedemann-Rautenstrauch syndrome or neonatal progeroid syndrome and review of the literature von Courtens, W, Nuytinck, L, Fricx, C, André, J, Vamos, E

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