Your search returned 5 results.

Results
	1.	Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment. [electronic resource] by Murthy, S K Nygren, A O H El Shakankiry, H M Schouten, J P Al Khayat, A I Ridha, A Al Ali, M T Producer: 20070402 In: Cytogenetic and genome research vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Single cell analysis of cancer cells using an improved RT-MLPA method has potential for cancer diagnosis and monitoring. [electronic resource] by Kvastad, L Werne Solnestam, B Johansson, E Nygren, A O Laddach, N Sahlén, P Vickovic, S Bendigtsen, Schirmer C Aaserud, M Floer, L Borgen, E Schwind, C Himmelreich, R Latta, D Lundeberg, J Producer: 20160909 In: Scientific reports vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Sequential gene promoter methylation during HPV-induced cervical carcinogenesis. [electronic resource] by Henken, F E Wilting, S M Overmeer, R M van Rietschoten, J G I Nygren, A O H Errami, A Schouten, J P Meijer, C J L M Snijders, P J F Steenbergen, R D M Producer: 20080116 In: British journal of cancer vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia. [electronic resource] by Beetz, C Nygren, A O H Schickel, J Auer-Grumbach, M Bürk, K Heide, G Kassubek, J Klimpe, S Klopstock, T Kreuz, F Otto, S Schüle, R Schöls, L Sperfeld, A-D Witte, O W Deufel, T Producer: 20070108 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation. [electronic resource] by Scott, R H Douglas, J Baskcomb, L Nygren, A O Birch, J M Cole, T R Cormier-Daire, V Eastwood, D M Garcia-Minaur, S Lupunzina, P Tatton-Brown, K Bliek, J Maher, E R Rahman, N Producer: 20080312 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)