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	821.	The Aarskog syndrome. [electronic resource] by Pedersen, J C Fryns, J P Bracke, P Geeraert, M Van der Berghe, H Producer: 19800926 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	822.	The elfin face syndrome and the short arm of chromosome 15. [electronic resource] by Fryns, J P van der Hauwaert, L G Dumoulin, M van den Berghe, H Producer: 19821218 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	823.	Apparent Greig cephalopolysyndactyly and sinus node disease. [electronic resource] by Fryns, J P De Waele, P Van der Hauwaert, L Van den Berghe, H Producer: 19930203 In: American journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	824.	Prenatal diagnosis of non-obstructive megacystis as part of the megacystis-microcolon-intestinal hypoperistalsis syndrome with favourable postnatal outcome. [electronic resource] by Witters, I Theyskens, C van Hoestenberghe, R Sieprath, P Gyselaers, W Fryns, J P Producer: 20011025 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	825.	The ICF syndrome: new case and update. [electronic resource] by De Ravel, T J Deckers, E Alliet, P L Petit, P Fryns, J P Producer: 20020723 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	826.	Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant. [electronic resource] by Vermeesch, J R Syrrou, M Salden, I Dhondt, F Matthijs, G Fryns, J-P Producer: 20021119 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	827.	A mosaic extra ring chromosome 4 in a female patient with postnatal overgrowth. [electronic resource] by Vermeesch, J R Petit, P Dutra, A Schröck, E Ried, T Fryns, J P Producer: 19991227 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	828.	Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male. [electronic resource] by Vermeesch, J R Duhamel, H Petit, P Falzetti, D Fryns, J P Marynen, P Producer: 20000216 In: Human genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	829.	Mathematical disabilities in children with velo-cardio-facial syndrome. [electronic resource] by De Smedt, B Swillen, A Devriendt, K Fryns, J P Verschaffel, L Ghesquière, P Producer: 20070426 In: Neuropsychologia vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	830.	Complex chromosome re-arrangement 45,X,t(Y;9) in a girl with sex reversal and mental retardation. [electronic resource] by de Ravel, T J L Fryns, J P Van Driessche, J Vermeesch, J R Producer: 20040728 In: American journal of medical genetics. Part A vol. 124A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	831.	Mathematical disabilities in young primary school children with velo-cardio-facial syndrome. [electronic resource] by De Smedt, B Swillen, A Devriendt, K Fryns, J P Verschaffel, L Ghesquiere, P Producer: 20070213 In: Genetic counseling (Geneva, Switzerland) vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	832.	The fetal phenotype in 2p trisomy. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, F Van den Berghe, K Van den Berghe, H Producer: 19870619 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	833.	The Roberts tetraphocomelia syndrome: identical limb defects in two siblings. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, P van den Berghe, K van den Berghe, H Producer: 19880211 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	834.	Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers. [electronic resource] by Boel, M Timmermans, J Emmery, L Dralands, G Fryns, J P Van den Berghe, H Producer: 19800215 In: Human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	835.	Mosaic tetrasomy 21 in severe mental handicap. [electronic resource] by Fryns, J P Petit, P Vinken, L Geutjens, J Marien, J Van den Berghe, H Producer: 19830214 In: European journal of pediatrics vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	836.	Phosphoserine phosphatase deficiency in a patient with Williams syndrome. [electronic resource] by Jaeken, J Detheux, M Fryns, J P Collet, J F Alliet, P Van Schaftingen, E Producer: 19970918 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)
	837.	Rearrangement of the human CDC5L gene by a t(6;19)(p21;q13.1) in a patient with multicystic renal dysplasia. [electronic resource] by Groenen, P M Vanderlinden, G Devriendt, K Fryns, J P Van de Ven, W J Producer: 19980806 In: Genomics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	838.	Oculo-auriculo-vertebral spectrum in Klinefelter syndrome. [electronic resource] by Garavelli, L Virdis, R Donadio, A Sigorini, M Banchini, G Balestrazzi, P Fryns, J P Producer: 20000106 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	839.	Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitus. [electronic resource] by Chabchoub, E Michils, G Vermeesch, J R De Cock, P Lagae, L Fryns, J P Producer: 20100514 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	840.	Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2)). [electronic resource] by Fryns, J P Bulcke, J Verdu, P Carton, H Kleczkowska, A Van den Berghe, H Producer: 19911220 In: American journal of medical genetics vol. 40 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.