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	801.	Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations. [electronic resource] by Vantrappen, G Rommel, N Swillen, A Cremers, C W Fryns, J P Devriendt, K Producer: 20031008 In: Acta oto-rhino-laryngologica Belgica vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	802.	Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29. [electronic resource] by Chabchoub, E Cogulu, O Durmaz, B Vermeesch, J R Ozkinay, F Fryns, J-P Producer: 20120717 In: Dermatology (Basel, Switzerland) vol. 223 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	803.	"Spontaneous" FRA16B is a hot spot for sister chromatid exchanges. [electronic resource] by Lukusa, T Meulepas, E Fryns, J P Van den Berghe, H Cassiman, J J Producer: 19911030 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	804.	A genetic diagnostic survey in an institutionalized population of 262 moderately mentally retarded patients: the Borgerstein experience. [electronic resource] by Fryns, J P Volcke, P H Haspeslagh, M Beusen, L Van den Berghe, H Producer: 19900514 In: Journal of mental deficiency research vol. 34 ( Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	805.	Ring chromosome 14. A distinct clinical entity. [electronic resource] by Fryns, J P Kubien, E Kleczkowska, A Nawrocka-Kanska, B Van den Berghe, H Producer: 19840607 In: Journal de genetique humaine vol. 31 Suppl 5 Availability: No items available. Save to lists Add to cart (remove)
	806.	Bloom's syndrome. Possible pitfalls in clinical diagnosis. [electronic resource] by Vanderschueren-Lodeweyckx, M Fryns, J P Van den Berghe, H Eggermont, E Eeckels, R Producer: 19840926 In: American journal of diseases of children (1960) vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	807.	Carpal and tarsal osteolysis. [electronic resource] by Fryns, J P Pedersen, J C Hauglustaine, D Michielsen, P Van den Berghe, H Producer: 19800926 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	808.	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)
	809.	Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy. [electronic resource] by Fryns, J P Emmery, L Timmermans, J Pedersen, J C van den Berghe, H Producer: 19801024 In: Journal de genetique humaine vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	810.	Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndrome. [electronic resource] by Wu, R Legius, E Robberecht, W Dumoulin, M Cassiman, J J Fryns, J P Producer: 19961120 In: Human mutation vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	811.	Severe intrauterine growth retardation, blepharophimosis, and cylindrical nose with midline groove: a new syndrome? [electronic resource] by de Die-Smulders, C E Droog, R P van Dijk, M Fryns, J P Producer: 19930810 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	812.	Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism. [electronic resource] by Devriendt, K Keymolen, K Roelen, L Van Goethem, G Meireleire, J Fryns, J P Producer: 20000802 In: Clinical dysmorphology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	813.	Second polar body inclusion results in diploid/triploid mixoploidy. [electronic resource] by Brems, H Vogels, A Ribai, P De Raedt, T Fryns, J P Legius, E Producer: 20040421 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	814.	The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15. [electronic resource] by Chabchoub, E Vermeesch, J R de Ravel, T de Cock, P Fryns, J-P Producer: 20080403 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	815.	Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21). [electronic resource] by Witters, I Balikova, I Cannie, M Devriendt, K De Catte, L Fryns, J P Producer: 20090330 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	816.	Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entity. [electronic resource] by Grubben, C de Cock, P Borghgraef, M van den Berghe, H Fryns, J P Producer: 19920824 In: Clinical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	817.	On the etiology of hearing loss in a population of 155 institutionalized children. [electronic resource] by Dereymaeker, A M Fryns, J P Ars, B Andrescescou, J Van den Berghe, H Producer: 19911206 In: Acta oto-rhino-laryngologica Belgica vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	818.	Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome. [electronic resource] by Curfs, L M Wiegers, A M Sommers, J R Borghgraef, M Fryns, J P Producer: 19920312 In: Clinical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	819.	Strengths and weaknesses in the cognitive profile of fra(X) patients. [electronic resource] by Curfs, L M Borghgraef, M Wiegers, A Schreppers-Tijdink, G A Fryns, J P Producer: 19900119 In: Clinical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	820.	Retinitis pigmentosa, hearing loss and vitiligo: report of two patients. [electronic resource] by Dereymaeker, A M Fryns, J P Ars, J Andresescu, J van den Berghe, H Producer: 19890920 In: Clinical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.