The probability of dizygosity of phenotypically concordant twins.

Por Meulepas, E, Vlietinck, R, van den Berghe, H
Publicado em 1988

A cluster of HTLV-1 associated tropical spastic paraparesis in Equateur (Zaire): ethnic and familial distribution.

Por Kayembe, K, Goubau, P, Desmyter, J, Vlietinck, R, Carton, H
Publicado em 1990

Utilisation and cost of professional care and assistance according to disability of patients with multiple sclerosis in Flanders (Belgium)

Por Carton, H, Loos, R, Pacolet, J, Versieck, K, Vlietinck, R
Publicado em 1998

X chromosome-inactivation patterns confirm the late timing of monoamniotic-MZ twinning.

Por Chitnis, S, Derom, C, Vlietinck, R, Derom, R, Monteiro, J, Gregersen, P K
Publicado em 1999

Commitment to X inactivation precedes the twinning event in monochorionic MZ twins.

Por Monteiro, J, Derom, C, Vlietinck, R, Kohn, N, Lesser, M, Gregersen, P K
Publicado em 1998

Significance of the Single Umbilical Artery: A Clinical, Radiological, Chromosomal, and Dermatoglyphic Study

Por Vlietinck, R. F., Thiery, M., Orye, E., De Clercq, A., Van Vaerenbergh, P.
Publicado em 1972

Genome wide scan in a Flemish inflammatory bowel disease population: support for the IBD4 locus, population heterogeneity, and epistasis

Por Vermeire, S, Rutgeerts, P, Van Steen, K, Joossens, S, Claessens, G, Pierik, M, Peeters, M, Vlietinck, R
Publicado em 2004

Zygosity determination in newborn twins using DNA variants.

Por Derom, C, Bakker, E, Vlietinck, R, Derom, R, Van den Berghe, H, Thiery, M, Pearson, P
Publicado em 1985

Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study

Por Lambrechts, D, Devriendt, K, Driscoll, D, Goldmuntz, E, Gewillig, M, Vlietinck, R, Collen, D, Carmeliet, P
Publicado em 2005

X chromosome inactivation patterns correlate with fetal-placental anatomy in monozygotic twin pairs: implications for immune relatedness and concordance for autoimmunity.

Por Trejo, V., Derom, C., Vlietinck, R., Ollier, W., Silman, A., Ebers, G., Derom, R., Gregersen, P. K.
Publicado em 1994

Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence.

Por Legius, E, Descheemaeker, M J, Steyaert, J, Spaepen, A, Vlietinck, R, Casaer, P, Demaerel, P, Fryns, J P
Publicado em 1995

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Por Yarden, J, Radojkovic, D, De Boeck, K, Macek, M, Zemkova, D, Vavrova, V, Vlietinck, R, Cassiman, J, Cuppens, H
Publicado em 2004

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Por Yarden, J, Radojkovic, D, De Boeck, K, Macek, M, Zemkova, D, Vavrova, V, Vlietinck, R, Cassiman, J, Cuppens, H
Publicado em 2005

The CAREGENE study: ACE gene I/D polymorphism and effect of physical training on aerobic power in coronary artery disease

Por Defoor, J, Vanhees, L, Martens, K, Matthijs, G, Van Vlerken, A, Zielinska, D, Schepers, D, Vlietinck, R, Fagard, R
Publicado em 2006

The Belgian PCB and dioxin incident of January-June 1999: exposure data and potential impact on health.

Por van Larebeke, N, Hens, L, Schepens, P, Covaci, A, Baeyens, J, Everaert, K, Bernheim, J L, Vlietinck, R, De Poorter, G
Publicado em 2001

Anticipation in familial Crohn's disease

Por Grandbastien, B, Peeters, M, Franchimont, D, Gower-Rousseau, C, Speckel, D, Rutgeerts, P, Belaiche, J, Cortot, A, Vlietinck, R, Colombel, J
Publicado em 1998

Epithelioid granulomas, pattern recognition receptors, and phenotypes of Crohn’s disease

Por Pierik, M, De Hertogh, G, Vermeire, S, Van Assche, G, Van Eyken, P, Joossens, S, Claessens, G, Vlietinck, R, Rutgeerts, P, Geboes, K
Publicado em 2005

Genome-wide linkage scan for maximum and length-dependent knee muscle strength in young men: significant evidence for linkage at chromosome 14q24.3

Por De Mars, G, Windelinckx, A, Huygens, W, Peeters, M W, Beunen, G P, Aerssens, J, Vlietinck, R, Thomis, M A I
Publicado em 2008

Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities

Por Souren, N. Y., Paulussen, A. D. C., Loos, R. J. F., Gielen, M., Beunen, G., Fagard, R., Derom, C., Vlietinck, R., Zeegers, M. P.
Publicado em 2007

Risks of multiple sclerosis in relatives of patients in Flanders, Belgium.

Por Carton, H, Vlietinck, R, Debruyne, J, De Keyser, J, D'Hooghe, M B, Loos, R, Medaer, R, Truyen, L, Yee, I M, Sadovnick, A D
Publicado em 1997