Segregation of the fragile X mutation from an affected male to his normal daughter
Willems, P J, Van Roy, B, De Boulle, K, Vits, L, Reyniers, E, Beck, O, Dumon, J E, Verkerk, A, Oostra, B
Published in Human molecular genetics (01.10.1992)
Published in Human molecular genetics (01.10.1992)
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Journal Article
Fryns syndrome without diaphragmatic hernia?
Willems, P J, Keersmaekers, G H, Dom, K E, Colpaert, C, Schatteman, E, Vergote, I B, Dumon, J E
Published in American journal of medical genetics (01.11.1991)
Published in American journal of medical genetics (01.11.1991)
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Journal Article
Fucosidosis revisited: a review of 77 patients
Willems, P J, Gatti, R, Darby, J K, Romeo, G, Durand, P, Dumon, J E, O'Brien, J S
Published in American journal of medical genetics (01.01.1991)
Published in American journal of medical genetics (01.01.1991)
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Journal Article
Fragile X trait in a large kindred: transmission also through normal males
Van Roy, B C, De Smedt, M C, Raes, R A, Dumon, J E, Leroy, J G
Published in Journal of medical genetics (01.08.1983)
Published in Journal of medical genetics (01.08.1983)
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Journal Article
Blomstrand lethal osteochondrodysplasia
Leroy, J G, Keersmaeckers, G, Coppens, M, Dumon, J E, Roels, H
Published in American journal of medical genetics (03.05.1996)
Published in American journal of medical genetics (03.05.1996)
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Acardiac amorphous twin with prune belly sequence in the co-twin
Buntinx, I M, Bourgeois, N, Buytaert, P M, Dumon, J E
Published in American journal of medical genetics (15.06.1991)
Published in American journal of medical genetics (15.06.1991)
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Tricho-rhino-phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24
Marchau, F E, Van Roy, B C, Parizel, P M, Lambert, J R, De Canck, I, Leroy, J G, Gevaert, C M, Willems, P J, Dumon, J E
Published in American journal of medical genetics (15.02.1993)
Published in American journal of medical genetics (15.02.1993)
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Journal Article
Two brothers with mental retardation discordant for the fragile-X syndrome
Van Roy, B C, Willems, P J, Vits, L J, Ceulemans, B P, Coucke, P J, Van der Auwera, B J, Lormans, J A, Dumon, J E
Published in American journal of medical genetics (01.05.1990)
Published in American journal of medical genetics (01.05.1990)
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Journal Article
Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy and Adrenomyeloneuropathy Present Within the Same Family
Willems, Patrick J, Vits, Lieve, Wanders, Ronald J. A, Coucke, Paul J, Van der Auwera, Bart J, Van Elsen, August F, Raeymaekers, Peter, Van Broeckhoven, Christine, Schutgens, Ruud B. H, Dacremont, Georges, Leroy, Jules G, Martin, Jean-Jacques, Dumon, Jan E
Published in Archives of neurology (Chicago) (01.06.1990)
Published in Archives of neurology (Chicago) (01.06.1990)
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Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis
Leroy, J G, Van Elsen, A F, Martin, J J, Dumon, J E, Hulet, A E, Okada, S, Navarro, C
Published in The New England journal of medicine (28.06.1973)
Published in The New England journal of medicine (28.06.1973)
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Journal Article
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
Willems, Patrick J., Dijkstra, Irene, Van der Auwera, Bart J., Vits, Lieve, Coucke, Paul, Raeymaekers, Peter, Van Broeckhoven, Christine, Consalez, Giacomo G., Freeman, Sallie B., Warren, Stephen T., Brouwer, Oebele F., Brunner, Han G., Renier, Willy O., Van Elsen, August F., Dumon, Jan E.
Published in Genomics (San Diego, Calif.) (01.10.1990)
Published in Genomics (San Diego, Calif.) (01.10.1990)
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