Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator von Lumaka, A., Cosemans, N., Lulebo Mampasi, A., Mubungu, G., Mvuama, N., Lubala, T., Mbuyi‐Musanzayi, S., Breckpot, J., Holvoet, M., de Ravel, T., Van Buggenhout, G., Peeters, H., Donnai, D., Mutesa, L., Verloes, A., Lukusa Tshilobo, P., Devriendt, K.

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Monitoring and modeling pesticide fate in surface waters at the catchment scale von Holvoet, Katrijn M.A., Seuntjens, Piet, Vanrolleghem, Peter A.

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females von Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M

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Harmonizing Exclusion under the Refugee Convention by Reference to the Evidentiary Standards of International Criminal Law von Holvoet, M.

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EP-1691 IORT and stray radiation: comparison of 2 commercial linacs von Stevens, P., Van Hoof, F., Holvoet, M., Messens, E., Grasso, L., De Stefano, S., Felici, G., Verellen, D.

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ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism von Esch, H Van, Poirier, K, Zegher, F de, Holvoet, M, Bienvenu, T, Chelly, J, Devriendt, K, Fryns, J-P

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females von Palmer, E.E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, Hilde, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H.-H, Delgado, M.R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M.P, Chung, W.K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B.M, Grange, D.K, Manwaring, L, Tolmie, J, Joss, S, DDD Study, Cobben, J.M, Duijkers, F.A.M, Goehringer, J.M, Challman, T.D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S.P, Niu, Z, Rosenfeld, J.A, Stankiewicz, P, Jentsch, T.J, Gecz, J, Field, M, Kalscheuer, V.M

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Extension of the River Water Quality Model No. 1 with the fate of pesticides von De Schepper, Veerle C. J., Holvoet, Katrijn M. A., Benedetti, Lorenzo, Seuntjens, Piet, Vanrolleghem, Peter A.

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Triplication of distal chromosome 10q von Devriendt, Koen, Matthijs, Gert, Holvoet, Maureen, Schoenmakers, Eric, Fryns, Jean-Pierre

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The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation von Devriendt, Koenraad, Holvoet, Maureen, De Mûelenaere, Alain, Fryns, Jean-Pierre

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Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1 von DE RAVEL, T J L, MATTHIJS, G, HOLVOET, M, WOUTERS, C, LEGIUS, E, FRYNS, J P

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Severe mental retardation : distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25 → qter deletion von LUKUSA, T, DEVRIENDT, K, HOLVOET, M, FRYNS, J. P

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Changements climatiques, aménagement de l’espace et transition urbanistique von Calenda

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Kleinschalig genormaliseerd wonen voor mensen met dementie, Het antwoord op 101 vragen von Spruytte, Nele, Declercq, Anja, Herbots, B, Holvoet, M, Elst, R, Van der Flaas, J, Molenberghs, C, Kuylen, L, Lecoutere, J, Van den Heuvel, B, Van Audenhove, Chantal

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X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family von Van Esch, Hilde, Zanni, Ginevra, Holvoet, Maureen, Borghgraef, Martine, Chelly, Jamel, Fryns, Jean-Pierre, Devriendt, Koenraad

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A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8 von Claeys, Ingrid, Holvoet, Maureen, Eyskens, Benedicte, Adriaensens, Peter, Gewillig, Marc, Fryns, Jean-Pierre, Devriendt, Koenraad

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Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome von Devriendt, K, Petit, P, Matthijs, G, Vermeesch, J R, Holvoet, M, De Muelenaere, A, Marynen, P, Cassiman, J J, Fryns, J P

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Partial DiGeorge syndrome in two patients with a 10p rearrangement von Van Esch, Hilde, Groenen, Peter, Daw, Sarah, Poffyn, Ann, Holvoet, Maureen, Scambler, Peter, Fryns, Jean-Pierre, Van de Ven, Wim, Devriendt, Koen

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Cri du chat syndrome: Changing phenotype in older patients von Van Buggenhout, G.J.C.M., Pijkels, E., Holvoet, M., Schaap, C., Hamel, B.C.J., Fryns, J.P.

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Follow-up of an adult with Keutel syndrome von Devriendt, Koen, Holvoet, Maureen, Fryns, Jean-Pierre

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