Resultats de la cerca - Proesmans, W

Nephronophthisis. per Proesmans, W, van Damme, B

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Renal and urological tract malformations caused by a 22q11 deletion. per Devriendt, K, Swillen, A, Fryns, J P, Proesmans, W, Gewillig, M

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Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis. per Devriendt, K, Matthijs, G, Claes, S, Legius, E, Proesmans, W, Cassiman, J J, Fryns, J P

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Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene. per van Lieburg, A. F., Verdijk, M. A., Knoers, V. V., van Essen, A. J., Proesmans, W., Mallmann, R., Monnens, L. A., van Oost, B. A., van Os, C. H., Deen, P. M.

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Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. per Schimmenti, L A, Cunliffe, H E, McNoe, L A, Ward, T A, French, M C, Shim, H H, Zhang, Y H, Proesmans, W, Leys, A, Byerly, K A, Braddock, S R, Masuno, M, Imaizumi, K, Devriendt, K, Eccles, M R

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Molecular analysis of SALL1 mutations in Townes-Brocks syndrome. per Kohlhase, J, Taschner, P E, Burfeind, P, Pasche, B, Newman, B, Blanck, C, Breuning, M H, ten Kate, L P, Maaswinkel-Mooy, P, Mitulla, B, Seidel, J, Kirkpatrick, S J, Pauli, R M, Wargowski, D S, Devriendt, K, Proesmans, W, Gabrielli, O, Coppa, G V, Wesby-van Swaay, E, Trembath, R C, Schinzel, A A, Reardon, W, Seemanova, E, Engel, W

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