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	1.	Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10). [electronic resource] by Erdel, M Schuffenhauer, S Buchholz, B Barth-Witte, U Köchl, S Utermann, B Duba, H C Utermann, G Producer: 19960712 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. [electronic resource] by Buiting, K Dittrich, B Gross, S Lich, C Färber, C Buchholz, T Smith, E Reis, A Bürger, J Nöthen, M M Barth-Witte, U Janssen, B Abeliovich, D Lerer, I van den Ouweland, A M Halley, D J Schrander-Stumpel, C Smeets, H Meinecke, P Malcolm, S Gardner, A Lalande, M Nicholls, R D Friend, K Schulze, A Matthijs, G Kokkonen, H Hilbert, P Van Maldergem, L Glover, G Carbonell, P Willems, P Gillessen-Kaesbach, G Horsthemke, B Producer: 19980813 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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