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Displaying 6 results.
    • Journal article
    S-100 Protein in Amniotic-fluid of Anencephalic Fetuses
    Sindic, Christian[UCL] Freund, M. Vanregemorter, N. Dumoulin, Christine[UCL] Masson, PL. (1984) Prenatal Diagnosis — Vol. 4, no. 4, p. 297-302 (1984)
    • Journal article
    A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophy
    Lissens, W. Vervoort, R Vanregemorter, N. VanBogaert, P Freund, M. Dumoulin, Christine[UCL] Seneca, S Liebaers, I. (1996) Journal of Inherited Metabolic Disease — Vol. 19, no. 6, p. 782-786 (1996)
    • Journal article
    Biochemical-diagnosis of a Fatal Case of Gunther Disease in a Newborn With Hydrops-fetalis
    Verstraeten, L. Vanregemorter, N. Pardou, A. Deverneuil, H. Dasilva, V. Rodesch, F. Vermeylen, D. Donner, C. Noël, JC. Nordmann, Y. Hassoun, A. (1993) European Journal of Clinical Chemistry and Clinical Biochemistry — Vol. 31, no. 3, p. 121-128 (1993)
    • Journal article
    Prenatal-diagnosis and Fetal Pathology of Partial Trisomy 20p - Monosomy 4p Resulting From Paternal Translocation
    Vamos, E. Pratola, D. Vanregemorter, N. Freund, M. Flamentdurand, J. Rodesch, F. (1985) Prenatal Diagnosis — Vol. 5, no. 3, p. 209-214 (1985)
    • Journal article
    Severe Smith-lemli-opitz Syndrome With Prolonged Survival and Lipid Abnormalities
    Pierquin, G. Peeters, Patrick[UCL] Roels, F. Vamos, E. Brucher, Jean-Marie[UCL] Tint, GS. Honda, A. Vanregemorter, N. (1995) American Journal of Medical Genetics — Vol. 56, no. 3, p. 276-280 (1995)
    • Journal article
    Partial Trisomy-3p in 2 Siblings - Clinical and Pathological Findings
    Vanregemorter, N. Vamos, E. Gillerot, Y. Viteux, V. Hayez, F. Pardou, A. Flamentdurand, J. (1983) European Journal of Pediatrics — Vol. 141, no. 1, p. 53-56 (1983)