Your search returned 10 results.

Results
	1.	Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defect. [electronic resource] by Buttiens, M Fryns, J P Producer: 19871001 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	X-linked mental retardation with marfanoid habitus. [electronic resource] by Fryns, J P Buttiens, M Producer: 19880202 In: American journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Chromosome X-linked mental retardation and marfanoid syndrome]. [electronic resource] by Fryns, J P Buttiens, M van den Berghe, H Producer: 19880725 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	4.	An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation. [electronic resource] by Buttiens, M Fryns, J P van den Berghe, H Producer: 19900119 In: Clinical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1. [electronic resource] by Fryns, J P Kleczkowska, A Buttiens, M Marien, P van den Berghe, H Producer: 19870212 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance. [electronic resource] by Buttiëns, M Fryns, J P Jonckheere, P Brouckmans-Buttiëns, K Van den Berghe, H Producer: 19851017 In: Human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Corpus callosum agenesis, spastic quadriparesis and irregular lining of the lateral ventricles on CT-scan. A distinct X-linked mental retardation syndrome? [electronic resource] by Vles, J S Fryns, J P Folmer, K Boon, P Buttiens, M Grubben, C Janevski, B Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	8.	Ring chromosome 15 syndrome. Further delineation of the adult phenotype. [electronic resource] by Fryns, J P Kleczkowska, A Buttiens, M Jonckheere, P Brouckmans-Buttiens, K van den Berghe, H Producer: 19860701 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	9.	Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation. [electronic resource] by Kleczkowska, A Fryns, J P Buttiens, M de Bisschop, F Emmery, L Van den Berghe, H Producer: 19870414 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Risperidone as add-on therapy in behavioural disturbances in mental retardation: a double-blind placebo-controlled cross-over study. [electronic resource] by Vanden Borre, R Vermote, R Buttiëns, M Thiry, P Dierick, G Geutjens, J Sieben, G Heylen, S Producer: 19930503 In: Acta psychiatrica Scandinavica vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)