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	361.	De novo 3q/7q translocation and associated interstitial 7q35 deletion. [electronic resource] by Fryns, J P Kleczkowska, A van den Berghe, H Producer: 19880407 In: Clinical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	362.	Hyperlaxity in males with Melnick-Needles syndrome. [electronic resource] by Fryns, J P Schinzel, A Van den Berghe, H Producer: 19880624 In: American journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	363.	High incidence of mental retardation in Turner syndrome patients with ring chromosome X formation. [electronic resource] by Fryns, J P Kleczkowska, A Van Den Berghe, H Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	364.	Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literature. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19900815 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	365.	On the variable effect of mosaic normal/balanced chromosomal rearrangements in man. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19901119 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	366.	The Greig polysyndactyly-craniofacial dysmorphism syndrome. [electronic resource] by Fryns, J P Coeck, W van den Berghe, H Producer: 19780218 In: European journal of pediatrics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	367.	Behavioral and emotional problems in youngsters with Prader-Willi syndrome. [electronic resource] by Curfs, L M Verhulst, F C Fryns, J P Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	368.	Intelligence and the fra(X) syndrome: a review. [electronic resource] by Curfs, L M Wiegers, A M Fryns, J P Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	369.	The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patients. [electronic resource] by Borghgraef, M Fryns, J P Van den Berghe, H Producer: 19920313 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	370.	Partial trisomy 17q. Karyotype: 46,XY,der(21),t(17;21)(q22;p13). [electronic resource] by Fryns, J P Parloir, C Van den Berghe, H Producer: 19791129 In: Human genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	371.	Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline development. [electronic resource] by Fryns, J P Delooz, J van den Berghe, H Producer: 19930309 In: Clinical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	372.	Familial infantile cortical hyperostosis. [electronic resource] by Emmery, L Timmermans, J Christens, J Fryns, J P Producer: 19840127 In: European journal of pediatrics vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	373.	The Coffin-Siris syndrome: report of a family and further delineation. [electronic resource] by Haspeslagh, M Fryns, J P van den Berghe, H Producer: 19850110 In: Clinical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	374.	Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19841226 In: Annales de genetique vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	375.	[46, XXip karyotype in a woman with normal stature and gonadal dysgenesis without other congenital anomalies]. [electronic resource] by Van den Berghe, H Fryns, J P Devos, F Producer: 19740528 In: Humangenetik vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	376.	Renovascular hypertension. Prospective diagnostic yield in a random access population. [electronic resource] by Van den Berghe, H Fryns, J P David, G Producer: 19740302 In: Humangenetik vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	377.	Malformative syndrome with ring chromosome 13. [electronic resource] by Fryns, J P Deoover, J Van den Berghe, H Producer: 19750421 In: Humangenetik vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	378.	Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23. [electronic resource] by Fryns, J P Strømme, P van den Berghe, H Producer: 19940209 In: Clinical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	379.	The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndrome. [electronic resource] by Smeets, E Fryns, J P Van den Berghe, H Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	380.	Renal agenesis and trisomy 22: case report and review. [electronic resource] by Van Buggenhout, G J Verbruggen, J Fryns, J P Producer: 19950830 In: Annales de genetique vol. 38 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.