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	1.	Familial partial distal 18q (18q22-18q23) trisomy. [electronic resource] by De Muelenaere, A Fryns, J P Van den Berghe, H Producer: 19811122 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	2.	The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation. [electronic resource] by Devriendt, K Holvoet, M De Mûelenaere, A Fryns, J P Producer: 20000428 In: Clinical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The 4p-syndrome in a 24-year-old female. [electronic resource] by Fryns, J P de Muelenaere, A Van den Berghe, H Producer: 19820420 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	4.	Distal 10p deletion syndrome. [electronic resource] by Fryns, J P De Muelenaere, A Van den Berghe, H Producer: 19811122 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	5.	Partial distal 12q trisomy. [electronic resource] by de Muelenaere, A Fryns, J P Van Den Berghe, H Producer: 19810613 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	6.	Interstitial deletion of the long arm of chromosome 15. [electronic resource] by Fryns, J P de Muelenaere, A van den Berghe, H Producer: 19820708 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	7.	9p Trisomy/18p distal monosomy and multiple cutaneous leiomyomata. Another specific chromosomal site (18pter) in dominantly inherited multiple tumors? [electronic resource] by Fryns, J P Haspeslagh, M de Mûelenaere, A van Den Berghe, H Producer: 19850906 In: Human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood. [electronic resource] by Fryns, J P de Muelenaere, A Pedersen, J Van Den Berghe, H Producer: 19801218 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	9.	Ring chromosome 14 syndrome. [electronic resource] by Fryns, J P Petit, P Kleczkowska, A De Muelenaere, A ven den Berghe, H Producer: 19821218 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	10.	Mental retardation with pterygia, shortness and distinct facial appearance. A new MCA/MR syndrome. [electronic resource] by Haspeslagh, M Fryns, J P de Mûelenaere, A Schautteet, L van Eeckhoutte, I van den Berghe, H Producer: 19860219 In: Clinical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. [electronic resource] by Devriendt, K Petit, P Matthijs, G Vermeesch, J R Holvoet, M De Muelenaere, A Marynen, P Cassiman, J J Fryns, J P Producer: 19970716 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)