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	61.	Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts. [electronic resource] by Kehrer-Sawatzki, H Moschgath, E Maier, C Legius, E Elgar, G Krone, W Producer: 20000727 In: Gene vol. 251 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1. [electronic resource] by Rutkowski, J L Wu, K Gutmann, D H Boyer, P J Legius, E Producer: 20000623 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	NRAS Mutations in Noonan Syndrome. [electronic resource] by Denayer, E Peeters, H Sevenants, L Derbent, M Fryns, J P Legius, E Publication details: Molecular syndromology Jun 2012 In: Molecular syndromology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Apparently new "anophthalmia-plus" syndrome in sibs. [electronic resource] by Fryns, J P Legius, E Moerman, P Vandenberghe, K Van den Berghe, H Producer: 19960129 In: American journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Ten base pair duplication in exon 38 of the NF1 gene. [electronic resource] by Legius, E Hall, B K Wallace, M R Collins, F S Glover, T W Producer: 19941011 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Erratum: Capturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study. [electronic resource] by Carlier, A Brems, H Ashbourn, J M A Nica, I Legius, E Geris, L Publication details: Scientific reports 06 2017 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Capturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study. [electronic resource] by Carlier, A Brems, H Ashbourn, J M A Nica, I Legius, E Geris, L Producer: 20161223 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Met>Val substitution in a highly conserved region of the pro-alpha1(I) collagen C-propeptide domain causes alternative splicing and a mild EDS/OI phenotype. [electronic resource] by Symoens, S Nuytinck, L Legius, E Malfait, F Coucke, P J De Paepe, A Producer: 20041221 In: Journal of medical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene. [electronic resource] by Legius, E Wu, R Eyssen, M Marynen, P Fryns, J P Cassiman, J J Producer: 19950918 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)
	70.	Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells. [electronic resource] by Teng, H Jorissen, M Van Poppel, H Legius, E Cassiman, J J Cuppens, H Producer: 19970326 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Holoprosencephaly and postaxial polydactyly with normal chromosomes. Another observation of a new malformation syndrome; a case report. [electronic resource] by Ramaekers, P R Legius, E Verloes, A Gillerot, Y Vandenberghe, K Fryns, J P Producer: 19900816 In: European journal of obstetrics, gynecology, and reproductive biology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndrome. [electronic resource] by Wu, R Legius, E Robberecht, W Dumoulin, M Cassiman, J J Fryns, J P Producer: 19961120 In: Human mutation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Exclusion of linkage to 14q23-24 in a family with Holt-Oram syndrome. [electronic resource] by Ruiz, J C Legius, E Cuppens, H Moens, P Marynen, P Cassiman, J J Producer: 19950216 In: Clinical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	A compound nucleotide repeat in the neurofibromatosis (NF1) gene. [electronic resource] by Andersen, L B Tarlé, S A Marchuk, D A Legius, E Collins, F S Producer: 19931004 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Second polar body inclusion results in diploid/triploid mixoploidy. [electronic resource] by Brems, H Vogels, A Ribai, P De Raedt, T Fryns, J P Legius, E Producer: 20040421 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	76.	MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families. [electronic resource] by Schrander-Stumpel, C Fryns, J Cassiman, J J Legius, E Spaepen, A Höweler, C J Producer: 19920428 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS. [electronic resource] by Swillen, A Devriendt, K Legius, E Eyskens, B Dumoulin, M Gewillig, M Fryns, J P Producer: 19970822 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)
	78.	Familial temporal lobe epilepsy with febrile seizures. [electronic resource] by Depondt, C Van Paesschen, W Matthijs, G Legius, E Martens, K Demaerel, P Wilms, G Producer: 20020524 In: Neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	PTPN11 mutations in LEOPARD syndrome. [electronic resource] by Legius, E Schrander-Stumpel, C Schollen, E Pulles-Heintzberger, C Gewillig, M Fryns, J-P 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)
	80.	Molecular and cytogenetic analysis of tumors in von Recklinghausen neurofibromatosis. [electronic resource] by Glover, T W Stein, C K Legius, E Andersen, L B Brereton, A Johnson, S Producer: 19910819 In: Genes, chromosomes & cancer vol. 3 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.