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Results: 101-115/115
Authors:
Devriendt, K
Matthijs, G
Holvoet, M
Schoenmakers, E
Fryns, JP
Citation: K. Devriendt et al., Triplication of distal chromosome 10q, J MED GENET, 36(3), 1999, pp. 242-245
Authors:
Decruyenaere, M
Evers-Kiebooms, G
Boogaerts, A
Cassiman, JJ
Cloostermans, T
Demyttenaere, K
Dom, R
Fryns, JP
Citation: M. Decruyenaere et al., Psychological functioning before predictive testing for Huntington's disease: the role of the parental disease, risk perception, and subjective proximity of the disease, J MED GENET, 36(12), 1999, pp. 897-905
Authors:
Moog, U
Maroteaux, P
Schrander-Stumpel, CTRM
van Ooij, A
Schrander, JJP
Fryns, JP
Citation: U. Moog et al., Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?, J MED GENET, 36(11), 1999, pp. 856-858
Authors:
De Smet, L
Fryns, JP
Citation: L. De Smet et Jp. Fryns, Symbrachydactyly involving both the hand and foot, CLIN GENET, 56(2), 1999, pp. 176-176
Authors:
Van Esch, H
Groenen, P
Daw, S
Poffyn, A
Holvoet, M
Scambler, P
Fryns, JP
Van de Ven, W
Devriendt, K
Citation: H. Van Esch et al., Partial DiGeorge syndrome in two patients with a 10p rearrangement, CLIN GENET, 55(4), 1999, pp. 269-276
Authors:
Lukusa, T
Van den Berghe, L
Smeets, E
Fryns, JP
Citation: T. Lukusa et al., Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome, ANN GENET, 42(4), 1999, pp. 215-220
Authors:
Lukusa, T
Devriendt, K
Fryns, JP
Citation: T. Lukusa et al., A 3p deletion syndrome in a child with both del(3)(p25 -> pter) and dup(17)(q23 -> qter), ANN GENET, 42(2), 1999, pp. 91-94
Authors:
Devriendt, K
Jaeken, J
Matthijs, G
Van Esch, H
Debeer, P
Gewillig, M
Fryns, JP
Citation: K. Devriendt et al., Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent ductusbotalli, AM J HU GEN, 65(1), 1999, pp. 249-251
Authors:
Devriendt, K
Matthijs, G
Van Dael, R
Gewillig, M
Eyskens, B
Hjalgrim, H
Dolmer, B
McGaughran, J
Brondum-Nielsen, K
Marynen, P
Fryns, JP
Vermeesch, JR
Citation: K. Devriendt et al., Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1, AM J HU GEN, 64(4), 1999, pp. 1119-1126
Authors:
Fryns, JP
Van Buggenhout, G
Citation: Jp. Fryns et G. Van Buggenhout, Structural chromosome rearrangements in couples with recurrent fetal wastage, EUR J OB GY, 81(2), 1998, pp. 171-176
Authors:
Witters, I
Van Buggenhout, G
Moerman, P
Fryns, JP
Citation: I. Witters et al., Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiography, PRENAT DIAG, 18(12), 1998, pp. 1304-1307
Authors:
Lukusa, T
Fryns, JP
Citation: T. Lukusa et Jp. Fryns, Syndrome of facial, oral, and digital anomalies due to 7q21.2 -> q22.1 duplication, AM J MED G, 80(5), 1998, pp. 454-458
Authors:
Swillen, A
Devriendt, K
Vantrappen, G
Vogels, A
Rommel, N
Fryns, JP
Eyskens, B
Gewillig, M
Dumoulin, M
Citation: A. Swillen et al., Familial deletions of chromosome 22q11: The Leuven experience, AM J MED G, 80(5), 1998, pp. 531-532
Authors:
van Lieshout, CFM
de Meyer, RE
Curfs, LMG
Koot, HM
Fryns, JP
Citation: Cfm. Van Lieshout et al., Problem behaviors and personality of children and adolescents with Prader-Willi Syndrome, J PED PSYCH, 23(2), 1998, pp. 111-120
Authors:
Lukusa, T
Van Buggenhout, G
Devriendt, K
Meireleire, J
Van Goethem, G
Roelen, L
Fryns, JP
Citation: T. Lukusa et al., Zygodactyly as the most striking physical anomaly in an adult male patientwith pure partial trisomy 1q., ANN GENET, 41(4), 1998, pp. 199-204