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Displaying 10 results.
    • Journal article
    Roberts-sc Phocomelia Syndrome With Exencephaly
    Verloes, A. Herens, C. Vanmaldergem, L. Retz, MC. Dodinval, P. (1989) Annales de génétique — Vol. 32, no. 3, p. 169-170 (1989)
    • Journal article
    Lethal Short-rib With Median Cleft and Without Polydactyly - a Fourth Case
    Vanmaldergem, L. Gillerot, Y. Salmin, E. Verloes, A. Koulischer, L. (1990) Pediatric Radiology : roentgenology, nuclear medicine, ultrasonics, CT, MRI — Vol. 20, no. 5, p. 367-368 (1990)
    • Journal article
    Holoprosencephaly and Postaxial Polydactyly With Normal Chromosomes - Another Observation of a New Malformation Syndrome - a Case-report
    Ramaekers, PR. Legius, Eric[UCL] Verloes, A. Gillerot, Y. Vandenberghe, K. Fryns, JP. (1990) European Journal of Obstetrics & Gynecology and Reproductive Biology — Vol. 36, no. 1-2, p. 161-165 (1990)
    • Journal article
    Microspherophakia-metaphyseal Dysplasia - a New Dominantly Inherited Bone Dysplasia With Severe Eye Involvement
    Verloes, A. Vanmaldergem, L. Demarneffe, P. Dufier, JL. Maroteaux, P. (1990) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 27, no. 7, p. 467-471 (1990)
    • Journal article
    Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers
    Verloes, A. Debauche, Christian[UCL] Verellen, Gaston[UCL] Temple, IK Hubert, AF Hope, P Gould, S Deville, JL Koulischer, L. Sokal, Etienne[UCL] (1996) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 33, no. 6, p. 444-449 (1996)
    • Journal article
    Trisomy 20q - a New Case and Further Phenotypic Delineation
    Herens, C. Verloes, A. Laloux, F. Vanmaldergem, L. (1990) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 37, no. 5, p. 363-366 (1990)