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	1.	5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability. [electronic resource] by Kleffmann, W Zink, A M Lee, J A Senderek, J Mangold, E Moog, U Rappold, G A Wohlleber, E Engels, H Producer: 20130118 In: Molecular syndromology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. [electronic resource] by Zink, A M Wohlleber, E Engels, H Rødningen, O K Ravn, K Heilmann, S Rehnitz, J Katzorke, N Kraus, C Blichfeldt, S Hoffmann, P Reutter, H Brockschmidt, F F Kreiß-Nachtsheim, M Vogt, P H Prescott, T E Tümer, Z Lee, J A Producer: 20140409 In: Molecular syndromology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing. [electronic resource] by Hoebel, A K Drichel, D van de Vorst, M Böhmer, A C Sivalingam, S Ishorst, N Klamt, J Gölz, L Alblas, M Maaser, A Keppler, K Zink, A M Dixon, M J Dixon, J Hemprich, A Kruse, T Graf, I Dunsche, A Schmidt, G Daratsianos, N Nowak, S Aldhorae, K A Nöthen, M M Knapp, M Thiele, H Gilissen, C Reutter, H Hoischen, A Mangold, E Ludwig, K U Producer: 20171002 In: Journal of dental research vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)