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Results:
1-8
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Results: 8
Authors:
Lukusa, T
Willekens, D
Lukusa, N
De Cock, P
Fryns, JP
Citation: T. Lukusa et al., Terminal 6q25.3 deletion and abnormal behaviour, GEN COUNSEL, 12(3), 2001, pp. 213-221
Authors:
Lukusa, T
Fryns, JP
Citation: T. Lukusa et Jp. Fryns, Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence, GEN COUNSEL, 11(2), 2000, pp. 119-126
Authors:
Lukusa, T
Devriendt, K
Holvoet, M
Fryns, JP
Citation: T. Lukusa et al., Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: Unusual chromosome 9 variant, AM J MED G, 91(3), 2000, pp. 192-197
Authors:
Lukusa, T
Devriendt, K
Jaeken, J
Fryns, JP
Citation: T. Lukusa et al., Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1 -> q35 due to maternal ins(14;2) translocation, CLIN DYSMOR, 8(1), 1999, pp. 47-51
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:
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:
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
Risultati:
1-8
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