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	1.	Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations. [electronic resource] by Kalz-Füller, B Sleegers, E Schwanitz, G Schubert, R Producer: 19990824 In: Clinical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The structures of the human neuronal nicotinic acetylcholine receptor beta2- and alpha3-subunit genes (CHRNB2 and CHRNA3). [electronic resource] by Rempel, N Heyers, S Engels, H Sleegers, E Steinlein, O K Producer: 19990209 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome. [electronic resource] by Horsthemke, B Maat-Kievit, A Sleegers, E van den Ouweland, A Buiting, K Lich, C Mollevanger, P Beverstock, G Gillessen-Kaesbach, G Schwanitz, G Producer: 19970221 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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