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	21.	Prenatal diagnosis of trisomy 21 between 1991 and 1999 in the Leuven Centre for Human Genetics: effect of triple test screening. [electronic resource] by Witters, I Legius, E Matthijs, G Fryns, J P Producer: 20030103 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	22.	Association between CAG repeat number in the androgen receptor and male infertility in a Belgian study. [electronic resource] by Legius, E Vanderschueren, D Spiessens, C D'Hooghe, T Matthijs, G Producer: 19991103 In: Clinical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Pneumosinus dilatans and orbital meningioma in neurofibromatosis type 2. [electronic resource] by Vauterin, T Mombaerts, I Jorissen, M Sciot, R Legius, E Producer: 20060511 In: B-ENT vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	24.	Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis. A new case of a newly recognized entity. [electronic resource] by Proesmans, W Legius, E Van Herck, K Van Damme, B Producer: 19901026 In: Pediatric nephrology (Berlin, Germany) vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia). [electronic resource] by Schollen, E Kjaergaard, S Legius, E Schwartz, M Matthijs, G Producer: 20000918 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)
	26.	The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profile. [electronic resource] by De Smet, L Legius, E Fabry, G Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	27.	Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult height. [electronic resource] by Legius, E Mulier, M Van Damme, B Fryns, J P Producer: 19940209 In: Clinical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Fine mapping of X-linked clasped thumb and mental retardation (MASA syndrome) in Xq28. [electronic resource] by Legius, E Kaepernick, L Higgins, J V Glover, T W Producer: 19940921 In: Clinical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Neuropsychological profile in adults with neurofibromatosis type 1 compared to a control group. [electronic resource] by Descheemaeker, M-J Plasschaert, E Frijns, J-P Legius, E Producer: 20140325 In: Journal of intellectual disability research : JIDR vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. [electronic resource] by Legius, E Marchuk, D A Collins, F S Glover, T W Producer: 19930629 In: Nature genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Unequal meiotic crossover: a frequent cause of NF1 microdeletions. [electronic resource] by López Correa, C Brems, H Lázaro, C Marynen, P Legius, E Producer: 20010607 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation. [electronic resource] by Legius, E Moerman, P Fryns, J P Vandenberghe, K Eggermont, E Producer: 19890420 In: American journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome. [electronic resource] by Fryns, J P Legius, E Demaerel, P van den Berghe, H Producer: 19970509 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	New findings in the behavioral profile of young FraX females. [electronic resource] by Borghgraef, M Umans, S Steyaert, J Legius, E Fryns, J P Producer: 19961213 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)
	35.	Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome. [electronic resource] by Vogels, A Matthijs, G Legius, E Devriendt, K Fryns, J-P Producer: 20030221 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Role of visual evoked potentials in the assessment and management of optic pathway gliomas in children. [electronic resource] by Van Mierlo, C Spileers, W Legius, E Casteels, I Cassiman, C Producer: 20140311 In: Documenta ophthalmologica. Advances in ophthalmology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion. [electronic resource] by Legius, E Baten, E Stul, M Marynen, P Cassiman, J J Producer: 19901106 In: Clinical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Schinzel acrocallosal syndrome: a variant example of the Greig syndrome? [electronic resource] by Legius, E Fryns, J P Casaer, P Boel, M Eggermont, E Producer: 19860424 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	39.	MASA syndrome: new clinical features and linkage analysis using DNA probes. [electronic resource] by Schrander-Stumpel, C Legius, E Fryns, J P Cassiman, J J Producer: 19910305 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Intraparenchymal meningioma in a 14-month-old infant: case report. [electronic resource] by Legius, E Vles, J S Casaer, P Plets, C Dom, R Producer: 19860429 In: Brain & development vol. 7 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.