K. Devriendt
Center for Human Genetics
University Hospital Gasthuisberg
Leuven
Belgium
Name/email consistency: high
- Genetic control of intra-uterine growth. Devriendt, K. Eur. J. Obstet. Gynecol. Reprod. Biol. (2000)
- Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. Devriendt, K., Matthijs, G., Van Dael, R., Gewillig, M., Eyskens, B., Hjalgrim, H., Dolmer, B., McGaughran, J., Bröndum-Nielsen, K., Marynen, P., Fryns, J.P., Vermeesch, J.R. Am. J. Hum. Genet. (1999)
- Vesico-ureteral reflux: a genetic condition?. Devriendt, K., Groenen, P., Van Esch, H., van Dijck, M., Van de Ven, W., Fryns, J.P., Proesmans, W. Eur. J. Pediatr. (1998)
- Deletion in chromosome region 22q11 in a child with CHARGE association. Devriendt, K., Swillen, A., Fryns, J.P. Clin. Genet. (1998)
- Missense mutation and hexanucleotide duplication in the PAX2 gene in two unrelated families with renal-coloboma syndrome (MIM 120330). Devriendt, K., Matthijs, G., Van Damme, B., Van Caesbroeck, D., Eccles, M., Vanrenterghem, Y., Fryns, J.P., Leys, A. Hum. Genet. (1998)
- Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita. Devriendt, K., Matthijs, G., Legius, E., Schollen, E., Blockmans, D., van Geet, C., Degreef, H., Cassiman, J.J., Fryns, J.P. Am. J. Hum. Genet. (1997)
