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	101.	Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor. [electronic resource] by de Ravel, T J Legius, E Brems, H Van Hoestenberghe, R Gillis, P H Fryns, J P Producer: 20020312 In: Clinical dysmorphology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype. [electronic resource] by Witters, I Legius, E Devriendt, K Moerman, P Van Schoubroeck, D Van Assche, A Fryns, J P Producer: 20011018 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool? [electronic resource] by Cassiman, C Casteels, I Jacob, J Plasschaert, E Brems, H Dubron, K Keer, K V Legius, E Producer: 20170630 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	TP53 mutations are frequent in malignant NF1 tumors. [electronic resource] by Legius, E Dierick, H Wu, R Hall, B K Marynen, P Cassiman, J J Glover, T W Producer: 19941104 In: Genes, chromosomes & cancer vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Diaphragmatic hernia in Denys-Drash syndrome. [electronic resource] by Devriendt, K Deloof, E Moerman, P Legius, E Vanhole, C de Zegher, F Proesmans, W Devlieger, H Producer: 19950921 In: American journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH). [electronic resource] by Witters, Ingrid Devriendt, K Legius, E Matthijs, G Van Schoubroeck, D Van Assche, F A Fryns, Jean-Pierre Producer: 20020412 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Correlations between triplet repeat expansion and clinical features in Huntington's disease. [electronic resource] by Claes, S Van Zand, K Legius, E Dom, R Malfroid, M Baro, F Godderis, J Cassiman, J J Producer: 19950912 In: Archives of neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence. [electronic resource] by Legius, E Descheemaeker, M J Steyaert, J Spaepen, A Vlietinck, R Casaer, P Demaerel, P Fryns, J P Producer: 19960118 In: Journal of neurology, neurosurgery, and psychiatry vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2) [electronic resource] by Legius, E Fryns, J P Eyskens, B Eggermont, E Desmet, V de Bethune, G Van den Berghe, H Producer: 19900607 In: American journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients. [electronic resource] by Spaepen, M Vankeirsbilck, B Van Opstal, S Tejpar, S Van Cutsem, E Geboes, K Legius, E Matthijs, G Producer: 20060816 In: Familial cancer vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Unusual molecular findings in autosomal recessive spinal muscular atrophy. [electronic resource] by Matthijs, G Schollen, E Legius, E Devriendt, K Goemans, N Kayserili, H Apäk, M Y Cassiman, J J Producer: 19961203 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions. [electronic resource] by Vanneste, E Melotte, C Debrock, S D'Hooghe, T Brems, H Fryns, J P Legius, E Vermeesch, J R Producer: 20090825 In: Human reproduction (Oxford, England) vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene. [electronic resource] by Moalem, S Brouillard, P Kuypers, D Legius, E Harvey, E Taylor, G Francois, M Vikkula, M Chitayat, D Producer: 20151215 In: Clinical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Linkage analysis in three families with nonspecific X-linked mental retardation. [electronic resource] by Claes, S Gu, X X Legius, E Lorenzetti, E Marynen, P Fryns, J P Cassiman, J J Raeymaekers, P Producer: 19961120 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Hydrocephalus and spastic paraplegia result from a donor splice site mutation (2872 + 1G to A) in the L1CAM gene in a Venezuelan pedigree. [electronic resource] by Claes, S Aguirre, T Simosa, V Bustos, T Lander, R Piras, M Legius, E Cassiman, J J Raeymaekers, P Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Psychotic disorders in Prader-Willi syndrome. [electronic resource] by Vogels, A De Hert, M Descheemaeker, M J Govers, V Devriendt, K Legius, E Prinzie, P Fryns, J P Producer: 20050222 In: American journal of medical genetics. Part A vol. 127A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Cognitive function and academic performance in neurofibromatosis. 1: consensus statement from the NF1 Cognitive Disorders Task Force. [electronic resource] by North, K N Riccardi, V Samango-Sprouse, C Ferner, R Moore, B Legius, E Ratner, N Denckla, M B Producer: 19970515 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	NF1-related locus on chromosome 15. [electronic resource] by Legius, E Marchuk, D A Hall, B K Andersen, L B Wallace, M R Collins, F S Glover, T W Producer: 19920922 In: Genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Gender-specific regional changes in genetic structure of muscularity in early adolescence. [electronic resource] by Loos, R Thomis, M Maes, H H Beunen, G Claessens, A L Derom, C Legius, E Derom, R Vlietinck, R Producer: 19970822 In: Journal of applied physiology (Bethesda, Md. : 1985) vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions. [electronic resource] by Lopez Correa, C Brems, H Lázaro, C Estivill, X Clementi, M Mason, S Rutkowski, J L Marynen, P Legius, E Producer: 20000106 In: Human mutation vol. 14 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.