Your search returned 148 results.

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	81.	The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. [electronic resource] by Swillen, A Devriendt, K Legius, E Prinzie, P Vogels, A Ghesquière, P Fryns, J P Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	82.	Predictive genetic testing for hereditary breast and ovarian cancer: psychological distress and illness representations 1 year following disclosure. [electronic resource] by Claes, E Evers-Kiebooms, G Denayer, L Decruyenaere, M Boogaerts, A Philippe, K Legius, E Producer: 20060303 In: Journal of genetic counseling vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Psychosocial aspects of familial breast and ovarian cancer: psychological guidelines for genetic testing. [electronic resource] by Decruyenaere, M Evers-Kiebooms, G Claes, E Denayer, L Welkenhuysen, M Legius, E Demyttenaere, K Producer: 20000120 In: Disease markers vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1. [electronic resource] by De Ravel, T J Matthijs, G Holvoet, M Wouters, C Legius, E Fryns, J P Producer: 20001207 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Predictive and prenatal genetic testing in hereditary ataxia's. Report of a workshop. [electronic resource] by van den Kerchove, M Evers-Kiebooms, G Kreuz, F Kroebel, D Legius, E Morgan, M Producer: 19970318 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	86.	Lethal osteochondrodysplasia and de novo autosomal translocation involving the long arm of chromosome 4. [electronic resource] by Fryns, J P Legius, E Van den Berghe, H Moerman, P Vandenberghe, K Maroteaux, P Producer: 19941018 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Intelligence in individuals with a neurofibromatosis type 1 microdeletion. [electronic resource] by Descheemaeker, M J Roelandts, K De Raedt, T Brems, H Fryns, J P Legius, E Producer: 20050411 In: American journal of medical genetics. Part A vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Predictive testing for hereditary breast and ovarian cancer: a psychological framework for pre-test counselling. [electronic resource] by Decruyenaere, M Evers-Kiebooms, G Denayer, L Welkenhuysen, M Claes, E Legius, E Demyttenaere, K Producer: 20000512 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Opitz C syndrome and pseudohypoaldosteronism. [electronic resource] by De Koster, J Legius, E de Zegher, F Devlieger, H Fryns, J P Eggermont, E Producer: 19910125 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents. [electronic resource] by Vogels, A Devriendt, K Legius, E Decock, P Marien, J Hendrickx, G Fryns, J P Producer: 19990414 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	91.	De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia. [electronic resource] by Legius, E Wlodarska, I Selleri, L Evans, G A Wu, R Smet, G Fryns, J P Producer: 19961210 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis. [electronic resource] by Devriendt, K Matthijs, G Claes, S Legius, E Proesmans, W Cassiman, J J Fryns, J P Producer: 19970729 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Consecutive glioblastoma and B cell non-Hodgkin's lymphoma in a young child with von Recklinghausen's Neurofibromatosis. [electronic resource] by Uyttebroeck, A Legius, E Brock, P Van de Cassey, W Casaer, P Casteels-Van Daele, M Producer: 19941216 In: Medical and pediatric oncology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation. [electronic resource] by Tabaku, M Legius, E Robberecht, W Sciot, R Fryns, J P Cassiman, J J Matthijs, G Producer: 20000106 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	95.	Possible association of CD3 and CD4 polymorphisms with insulin-dependent diabetes mellitus (IDDM). [electronic resource] by Ghabanbasani, M Z Buyse, I Legius, E Decorte, R Marynen, P Bouillon, R Cassiman, J J Producer: 19941013 In: Clinical and experimental immunology vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Germline mutations in NF1 patients with malignancies. [electronic resource] by Wu, R López-Correa, C Rutkowski, J L Baumbach, L L Glover, T W Legius, E Producer: 20000201 In: Genes, chromosomes & cancer vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	97.	Risk-reducing mastectomy in BRCA carriers: survival is not the issue. [electronic resource] by Neven, P Punie, K Wildiers, H Willers, N Van Ongeval, C Van Buggenhout, G Legius, E Producer: 20200916 In: Breast cancer research and treatment vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders. [electronic resource] by Vogels, Annick Van Den Ende, Jenneke Keymolen, Kathelijne Mortier, Geert Devriendt, Koen Legius, E Fryns, J P Producer: 20041106 In: European journal of human genetics : EJHG vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS. [electronic resource] by Ruiz, J C Cuppens, H Legius, E Fryns, J P Glover, T Marynen, P Cassiman, J J Producer: 19951122 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Cohen syndrome: the clinical symptoms and stigmata at a young age. [electronic resource] by Fryns, J P Legius, E Devriendt, K Meire, F Standaert, L Baten, E Van den Berghe, H Producer: 19961203 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 148 results.