Your search returned 10 results.

Results
	1.	Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1. [electronic resource] by Messiaen, L M Wimmer, K Producer: 20060417 In: Journal of medical genetics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	2.	Qualitative and quantitative analysis of tumour invasion in vivo and in vitro. [electronic resource] by Mareel, M M Van Roy, F M Messiaen, L M Boghaert, E R Bruyneel, E A Producer: 19881212 In: Journal of cell science. Supplement vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Unilateral vestibular schwannoma and meningiomas in a patient with PIK3CA-related segmental overgrowth: Co-occurrence of mosaicism for 2 rare disorders. [electronic resource] by Mills, J R Moyer, A M Kipp, B R Poplawski, A B Messiaen, L M Babovic-Vuksanovic, D Producer: 20180806 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. [electronic resource] by Messiaen, L M Callens, T Mortier, G Beysen, D Vandenbroucke, I Van Roy, N Speleman, F Paepe, A D Producer: 20000811 In: Human mutation vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome? [electronic resource] by Mortier, G R Messiaen, L M Espeel, M Smets, K J Vanzieleghem, B D Roels, F De Paepe, A M Producer: 19990105 In: Pediatric radiology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Gonosomal mosaicism for an NF1 deletion in a sperm donor: evidence of the need for coordinated, long-term communication of health information among relevant parties. [electronic resource] by Callum, P Messiaen, L M Bower, P V Skovby, F Iger, J Timshel, S Sims, C A Falk, R E Producer: 20130109 In: Human reproduction (Oxford, England) vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts. [electronic resource] by Sharp, A M Messiaen, L M Page, G Antignac, C Gubler, M-C Onuchic, L F Somlo, S Germino, G G Guay-Woodford, L M Producer: 20060803 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing. [electronic resource] by Messiaen, L M Callens, T Roux, K J Mortier, G R De Paepe, A Abramowicz, M Pericak-Vance, M A Vance, J M Wallace, M R Producer: 20010419 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship? [electronic resource] by Bertola, D R Pereira, A C Brasil, A C Suzuki, L Leite, C Falzoni, R Tannuri, U Poplawski, A B Janowski, K M Kim, C A Messiaen, L M Producer: 20130703 In: Clinical genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. [electronic resource] by Beysen, D Raes, J Leroy, B P Lucassen, A Yates, J R W Clayton-Smith, J Ilyina, H Brooks, S Sklower Christin-Maitre, S Fellous, M Fryns, J P Kim, J R Lapunzina, P Lemyre, E Meire, F Messiaen, L M Oley, C Splitt, M Thomson, J Van de Peer, Y Veitia, R A De Paepe, A De Baere, E Producer: 20050923 In: American journal of human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)