Presence of δ-(l-α-Aminoadipyl)-l-Cysteinyl-d-Valine in Fermentations of Penicillium chrysogenum

Tekijä Adriaens, P., Meesschaert, B., Wuyts, W., Vanderhaeghe, H., Eyssen, H.
Julkaistu 1975

The world is not enough – the value of increasing registry data in idiopathic pulmonary fibrosis

Tekijä Moor, C. C., Kreuter, M., Luppi, F., Wuyts, W. A.
Julkaisussa Respir Res (2020)

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

Tekijä Wuyts, W., Cleiren, E., Homfray, T., Rasore-Quartino, A., Vanhoenacker, F., Van Hul, W.
Julkaistu 2000

Intima Sarcoma of the Pulmonary Artery Mimicking Takayasu Disease

Tekijä Belge, C., Renckens, I., Van Puijenbroek, R., Wuyts, W., Meyns, B., Delcroix, M.
Julkaistu 2011

Cost-Effectiveness Analysis of Nintedanib Versus Pirfenidone in Idiopathic Pulmonary Fibrosis in Belgium

Tekijä Rinciog, C., Diamantopoulos, A., Gentilini, A., Bondue, B., Dahlqvist, C., Froidure, A., Wuyts, W. A., Soulard, S.
Julkaisussa Pharmacoecon Open (2020)

Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21.

Tekijä Van Hul, W, Bollerslev, J, Gram, J, Van Hul, E, Wuyts, W, Benichou, O, Vanhoenacker, F, Willems, P J
Julkaistu 1997

A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis

Tekijä Xiao, C Y, Wang, J, Zhang, S Z, Hul, W Van, Wuyts, W, Qiu, W M, Wu, H, Zhang, G
Julkaistu 2001

KRAS mutation detection and prognostic potential in sporadic colorectal cancer using high-resolution melting analysis

Tekijä Deschoolmeester, V, Boeckx, C, Baay, M, Weyler, J, Wuyts, W, Van Marck, E, Peeters, M, Lardon, F, Vermorken, J B
Julkaistu 2010

EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

Tekijä Bovée, J V, Cleton-Jansen, A M, Wuyts, W, Caethoven, G, Taminiau, A H, Bakker, E, Van Hul, W, Cornelisse, C J, Hogendoorn, P C
Julkaistu 1999

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm...

Tekijä Bartsch, O., Wuyts, W., Van Hul, W., Hecht, J. T., Meinecke, P., Hogue, D., Werner, W., Zabel, B., Hinkel, G. K., Powell, C. M., Shaffer, L. G., Willems, P. J.
Julkaistu 1996

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease

Tekijä Balemans, W, Patel, N, Ebeling, M, Van Hul, E, Wuyts, W, Lacza, C, Dioszegi, M, Dikkers, F, Hildering, P, Willems, P, Verheij, J, Lindpaintner, K, Vickery, B, Foernzler, D, Van Hul, W
Julkaistu 2002

Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.

Tekijä Wuyts, W, Van Hul, W, De Boulle, K, Hendrickx, J, Bakker, E, Vanhoenacker, F, Mollica, F, Lüdecke, H J, Sayli, B S, Pazzaglia, U E, Mortier, G, Hamel, B, Conrad, E U, Matsushita, M, Raskind, W H, Willems, P J
Julkaistu 1998

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai...

Tekijä del Castillo, F J, Rodriguez-Ballest..., M, Alvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M, Marlin, S, Pandya, A, Shahin, H, Siemering, K, Weil, D, Wuyts, W, Aguirre, L, Martin, Y, Moreno-Pelayo, M, Villamar, M, Avraham, K, Dahl, H, Kanaan, M, Nance, W, Petit, C, Smith, R, Van Camp, G, Sartorato, E, Murgia, A, Moreno, F, del Castillo, I
Julkaistu 2005