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	1.	Is cancer risk related to genes for steroid receptors and estrogen metabolism? [electronic resource] by Legius, E Producer: 20070315 In: International journal of gynecological cancer : official journal of the International Gynecological Cancer Society vol. 16 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Four new DNA variants in the NF1 coding region. [electronic resource] by Wu, R Legius, E Producer: 20001121 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	3.	Schematic representation of NF-1 clinical features in French. [electronic resource] by Legius, E Fryns, J P Producer: 19900614 In: Neurofibromatosis vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	4.	Visual loss as the presenting sign of Jeune syndrome. [electronic resource] by Casteels, I Demandt, E Legius, E Producer: 20010126 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Sodium valproate, pregnancy, and infantile fatal liver failure. [electronic resource] by Legius, E Jaeken, J Eggermont, E Producer: 19880203 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome? [electronic resource] by Devriendt, K Legius, E Fryns, J P Producer: 19960919 In: American journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Multifocal glomus tumours of the fingers in two patients with neurofibromatosis type 1. [electronic resource] by De Smet, L Sciot, R Legius, E Producer: 20020903 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Clinical and molecular aspects of RAS related disorders. [electronic resource] by Denayer, E de Ravel, Th Legius, E Producer: 20081231 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Patient with the combination of Klippel-Feil anomaly, partial agenesis of the sacrum, bladder incontinence, and unilateral hydronephrosis. [electronic resource] by Legius, E Fryns, J P Eggermont, E Producer: 19900606 In: Journal of craniofacial genetics and developmental biology vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	10.	Skin pigmentation anomalies in ring chromosome 13. [electronic resource] by Fryns, J P Devriendt, K Legius, E Producer: 19980922 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	11.	Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum: an example of the variable clinical spectrum of the Acrocallosal syndrome? [electronic resource] by Fryns, J P Devriendt, K Legius, E Producer: 19970922 In: Clinical dysmorphology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Clinical aspects of the MASA syndrome in a large family, including expressing females. [electronic resource] by Kaepernick, L Legius, E Higgins, J Kapur, S 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)
	13.	Comparative study of the ophthalmological examinations in neurofibromatosis type 1. Proposal for a new screening algorithm. [electronic resource] by Caen, S Cassiman, C Legius, E Casteels, I Producer: 20160407 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Unilateral Coats'-like disease and an intragenic deletion in the TERC gene: A case report. [electronic resource] by Peene, G Smets, E Legius, E Cassiman, C Producer: 20190311 In: Ophthalmic genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene. [electronic resource] by Steyaert, J Borghgraef, M 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)
	16.	Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome. [electronic resource] by Legius, E Fryns, J P Van den Berghe, H Producer: 19900726 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Chromosomal mosaicism limited to fibroblasts and MCA/MR syndrome with fetal hypokinesia of central nervous origin. [electronic resource] by Fryns, J P Legius, E Van den Berghe, H Producer: 19941230 In: Annales de genetique vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	18.	Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family. [electronic resource] by Legius, E Schollen, E Matthijs, G Fryns, J P Producer: 19981110 In: European journal of human genetics : EJHG vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome? [electronic resource] by Legius, E Fryns, J P Van den Berghe, H Producer: 19891003 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defect. [electronic resource] by Petit, P Moerman, P Legius, E Fryns, J P Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 148 results.