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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:
Fryns, JP
De Cock, P
Citation: Jp. Fryns et P. De Cock, MCA/MR syndrome with occipital scalp defect and valvular pulmonary stenosis: A cryptic 7pter duplication/18qter deficiency, GEN COUNSEL, 12(1), 2001, pp. 103-104
Authors:
Willekens, D
De Cock, P
Fryns, JP
Citation: D. Willekens et al., Three young children with Smith-Magenis syndrome: Their distinct, recognisable behavioural phenotype as the most important clinical symptoms, GEN COUNSEL, 11(2), 2000, pp. 103-110
Authors:
Potgieter, S
Matthijs, G
De Cock, P
Fryns, JP
Citation: S. Potgieter et al., Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7, EUR J PED, 159(12), 2000, pp. 929-929
Authors:
De Cock, P
Van Ginkel, CJW
Faber, WR
Bruynzeel, DP
Citation: P. De Cock et al., Occupational airborne allergic contact dermatitis from sawdust in livestock sheds, CONTACT DER, 42(2), 2000, pp. 113-113
Authors:
Molenaers, G
Desloovere, K
Eyssen, M
Decat, J
Jonkers, I
De Cock, P
Citation: G. Molenaers et al., Botulinum toxin type A treatment of cerebral palsy: an integrated approach, EUR J NEUR, 6, 1999, pp. S51-S57
Authors:
Molenaers, G
Eyssen, M
Desloovere, K
Jonkers, I
De Cock, P
Citation: G. Molenaers et al., A multilevel approach to botulinum toxin type A treatment of the (ilio)psoas in spasticity in cerebral palsy, EUR J NEUR, 6, 1999, pp. S59-S62
Authors:
Stiers, P
De Cock, P
Vandenbussche, E
Citation: P. Stiers et al., Separating visual perception and non-verbal intelligence in children with early brain injury, BRAIN DEVEL, 21(6), 1999, pp. 397-406
Risultati:
1-8
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