المؤلفون: Witters, I.^Aff00071, Fryns, J. P.^Aff00071

المساهمون: de Baat, C., editor^Aff1, Allard, R. H. B., editor^Aff2, Aps, J. K. M., editor^{Aff3, Aff4}, Duyck, J., editor^Aff5, Fokkema, S. J., editor^Aff6, Jacobs, R., editor^Aff7, Vissink, A., editor^Aff8

المصدر: Het Tandheelkundig Jaar 2010. :71-77

المؤلفون: De Smedt, Bert, Devriendt, K., Fryns, J. -P, Vogels, A., Gewillig, M., Swillen, A.

المصدر: Journal of Intellectual Disability Research. Sep 2007 51(9):666-670.

Peer Reviewed: Y

Page Count: 5

Descriptors: Intelligence Quotient, Learning Disabilities, Cognitive Ability, Children, Genetics, Gender Differences, Heart Disorders, Mental Disorders, Foreign Countries

مصطلحات جغرافية: Belgium

المؤلفون: Maes, B., Fryns, J. P., Ghesquiere, P., Borghgraef, M.

المصدر: Mental Retardation. Jun 2000 38(3):207-215.

Peer Reviewed: Y

Page Count: 9

Descriptors: Adults, Check Lists, Children, Clinical Diagnosis, Diagnostic Tests, Disability Identification, Males, Mental Retardation, Test Reliability, Test Validity

المؤلفون: Evers-Kiebooms, G., Nys, K., Decruyenaere, M., Witters, I., Fryns, J.-P.

المصدر: Community Genetics, 2001 Jan 01. 4(1), 43-49.

URL الوصول: https://www.jstor.org/stable/26664527

المؤلفون: Van Buggenhout, G.J.C.M., Trommelen, J.C.M., Brunner, H.G., Hamel, B.C.J., Fryns, J.-P.

المصدر: Community Genetics, 2001 Jan 01. 4(2), 109-122.

URL الوصول: https://www.jstor.org/stable/26664541

المؤلفون: Laumonnier, F^{Aff1, Aff2, Aff3, IDmp200914_cor1}, Shoubridge, C, Antar, C^{Aff1, Aff2, Aff3, Aff5}, Nguyen, L S, Van Esch, H, Kleefstra, T, Briault, S^{Aff1, Aff2, Aff3, Aff8}, Fryns, J P, Hamel, B, Chelly, J, Ropers, H H, Ronce, N^{Aff1, Aff2, Aff3, Aff5}, Blesson, S, Moraine, C^{Aff1, Aff2, Aff4}, Gécz, J^{Aff4, Aff11, Aff12}, Raynaud, M^{Aff1, Aff2, Aff3, Aff5}

المصدر: Molecular Psychiatry. 15(7):767-776

المؤلفون: Poirier, K., Lacombe, D., Gilbert-Dussardier, B., Raynaud, M., Desportes, V., de Brouwer, A. P. M., Moraine, C., Fryns, J. P., Ropers, H. H., Beldjord, C., Chelly, J., Bienvenu, T.

المصدر: Neurogenetics. March 2006 7(1):39-46

المؤلفون: Peeters, H., Debeer, P., Bairoch, A., Wilquet, V., Huysmans, C., Parthoens, E., Fryns, J. P., Gewillig, M., Nakamura, Y., Niikawa, N., Van de Ven, W., Devriendt, K.

المصدر: Human Genetics. May 2003 112(5-6):573-580

المؤلفون: Knopf, C., Rod, R., Jaeken, J., Berant, M., Van Schaftingen, E., Fryns, J. P., Brill-Zamir, R., Gershoni-Baruch, R., Lischinsky, S., Mandel, H.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. June 2000 23(4):399-403

المؤلفون: Vermeesch, J.R., Duhamel, H., Petit, P., Falzetti, D., Fryns, J.-P., Marynen, P.

المصدر: Human Genetics. December 1999 105(6):611-618