MspI RFLP in the L1 CAM gene in Xq28

od Willems, P.J., Vits, L., De Boulle, K.
Wydane 1991

Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome.

od Superti-Furga, A, Raghunath, M, Willems, P J
Wydane 1992

Antibody formation in the mouse induced by hapten-carrier complexes.

od Snippe, H, Graven, W G, Willems, P J
Wydane 1975

Nonsyndromic hearing impairment: unparalleled heterogeneity.

od Van Camp, G, Willems, P J, Smith, R J
Wydane 1997

Delayed hypersensitivity in the mouse induced by hapten-carrier complexes.

od Snippe, H, Willems, P J, Graven, W G, Kamp, E
Wydane 1975

Genotype-phenotype correlation in L1 associated diseases.

od Fransen, E, Van Camp, G, D'Hooge, R, Vits, L, Willems, P J
Wydane 1998

cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

od Davidson, J J, Ozçelik, T, Hamacher, C, Willems, P J, Francke, U, Kilimann, M W
Wydane 1992

The first 3,000 Non-Invasive Prenatal Tests (NIPT) with the Harmony test in Belgium and the Netherlands

od Willems, P.J., Dierickx, H., Vandenakker, ES., Bekedam, D., Segers, N., Deboulle, K., Vereecken, A.
Wydane 2014

BclI RFLP in fucosidase pseudogene (FUCA1P)

od Willems, P.J., Carritt, B., Coucke, P., Darby, J.K., Van Der Auwera, B.J., O'Brien, J.S.
Wydane 1990

A 5' splice site mutation in fucosidosis.

od Williamson, M, Cragg, H, Grant, J, Kretz, K, O'Brien, J, Willems, P J, Young, E, Winchester, B
Wydane 1993

Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency.

od Buntinx, I M, Willems, P J, Spitaels, S E, Van Reempst, P J, De Paepe, A M, Dumon, J E
Wydane 1991

Complete genomic structure and mutational spectrum of PHKA2 in patients with x-linked liver glycogenosis type I and II.

od Hendrickx, J, Lee, P, Keating, J P, Carton, D, Sardharwalla, I B, Tuchman, M, Baussan, C, Willems, P J
Wydane 1999

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

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

Pvu II RFLP at the human chromosome 1 alpha-L-fucosidase gene locus (FUCA1).

od Darby, J K, Johnsen, J, Nakashima, P, Willems, P J, O'Brien, J S, Fowler, M L, Shows, T B, Shooter, E M, Cavalli-Sforza, L L
Wydane 1986

Mutations and phenotype in isolated glycerol kinase deficiency.

od Walker, A. P., Muscatelli, F., Stafford, A. N., Chelly, J., Dahl, N., Blomquist, H. K., Delanghe, J., Willems, P. J., Steinmann, B., Monaco, A. P.
Wydane 1996

Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

od Van Hul, W, Balemans, W, Van Hul, E, Dikkers, F G, Obee, H, Stokroos, R J, Hildering, P, Vanhoenacker, F, Van Camp, G, Willems, P J
Wydane 1998

Identification of a mutation in the structural alpha-L-fucosidase gene in fucosidosis.

od Willems, P J, Darby, J K, DiCioccio, R A, Nakashima, P, Eng, C, Kretz, K A, Cavalli-Sforza, L L, Shooter, E M, O'Brien, J S
Wydane 1988

Noninvasive test for fragile X syndrome, using hair root analysis.

od Willemsen, R, Anar, B, De Diego Otero, Y, de Vries, B B, Hilhorst-Hofstee, Y, Smits, A, van Looveren, E, Willems, P J, Galjaard, H, Oostra, B A
Wydane 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...

od 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.
Wydane 1996

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

od Lench, N J, Markham, A F, Mueller, R F, Kelsell, D P, Smith, R J, Willems, P J, Schatteman, I, Capon, H, Van De Heyning, P J, Van Camp, G
Wydane 1998