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	681.	Diagnostic echographic findings in cryptophthalmos syndrome (Fraser syndrome). [electronic resource] by Fryns, J P van Schoubroeck, D Vandenberghe, K Nagels, H Klerckx, P Producer: 19970821 In: Prenatal diagnosis vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	682.	Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophy. [electronic resource] by Fryns, J P Van Lingen, C Devriendt, K Legius, E Raus, P Producer: 19980630 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	683.	Partial monosomy 11q and trisomy 12q: variable expression in two siblings. [electronic resource] by Lukusa, T Holvoet, M Vermeesch, J R Devriendt, K Fryns, J P Producer: 20031104 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	684.	Partial trisomy 11q syndrome (11q23.1-->11qter) due to de novo t (11q; 13q) detected by multicolor fluorescence in situ hybridisation. [electronic resource] by Utine, G E Thoelen, R Peeters, H Vermeesch, J Fryns, J P Producer: 20060215 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	685.	Hyperextension of the fetal head with sinus bradycardia in 22q11 deletion. [electronic resource] by Witters, I Peeters, H Van Holsbeke, C Gyselaers, W Fryns, J P Producer: 20100318 In: Genetic counseling (Geneva, Switzerland) vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	686.	A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities. [electronic resource] by Fryns, J P Moerman, F Goddeeris, P Bossuyt, C Van den Berghe, H Producer: 19791024 In: Human genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	687.	Unknown. The combination of vitiligo vulgaris with somatic and psychomotor retardation, cleft palate and facial dysmorphism: a distinct entity? [electronic resource] by Schrander-Stumpel, C T Theunissen, P M Hulsmans, R F Fryns, J P Producer: 19920421 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	688.	Distinct dysmorphic syndrome in a child with inverted distal 5q duplication. [electronic resource] by Fryns, J P Kleczkowska, A Borghgraef, M Raveschot, J Van den Berghe, H Producer: 19871207 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	689.	Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. [electronic resource] by Curfs, L M Schreppers-Tijdink, G Wiegers, A Borghgraef, M Fryns, J P Producer: 19890825 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	690.	A malformed newborn with 9p and 4q trisomy. [electronic resource] by Fryns, J P Azou, M Devliegher, H Eggermont, E van den Berghe, H Producer: 19810613 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	691.	Tetrasomy 9p: prenatal diagnosis and fetopathological findings in a second trimester male fetus. [electronic resource] by Van Hove, J Kleczkowska, A De Bruyn, M Bekaert, J Fryns, J P Producer: 19950309 In: Annales de genetique vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	692.	Confirmation of defective cholesterol biosynthesis in 2 previously described adult sibs with Smith-Lemli-Opitz syndrome. [electronic resource] by De Die-Smulders, C Van de Meer, S Spaapen, L Fryns, J P Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	693.	Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p. [electronic resource] by Fryns, J P Kleczkowska, A Devriendt, K Devliegher, H Van den Berghe, H Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	694.	Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings. [electronic resource] by Delooz, J Van den Berghe, H Swillen, A Kleczkowska, A Fryns, J P Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	695.	Sex chromosome pentasomy (49, XXXXY) presenting with generalized oedema and hypogenitalism at 12 weeks. [electronic resource] by Witters, I Moerman, P H Braet, P Van Schoubroeck, D Fryns, J P Producer: 20010726 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	696.	Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndrome. [electronic resource] by Rommel, N Vantrappen, G Swillen, A Devriendt, K Feenstra, L Fryns, J P Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	697.	Multiple congenital anomalies syndrome with multicystic renal dysplasia, postaxial polydactyly and lumbosacral meningocoele. Difficulties in nosological classification and genetic counseling. [electronic resource] by Witters, I Moerman, Ph Natens, R Van Assche, F A Fryns, J P Producer: 20030103 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	698.	NRAS Mutations in Noonan Syndrome. [electronic resource] by Denayer, E Peeters, H Sevenants, L Derbent, M Fryns, J P Legius, E Publication details: Molecular syndromology Jun 2012 In: Molecular syndromology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	699.	Sex chromatin and cytogenetic survey of 10417 adult males and 357 children institutionalized in Belgian institutions for mentally retarded patients. [electronic resource] by Cassiman, J J Fryns, J P De Roover, J Van den Berghe, H Producer: 19751107 In: Humangenetik vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	700.	46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit. [electronic resource] by Fryns, J P Kleczkowska, A Decock, P Massa, G van den Berghe, H Producer: 19930422 In: Annales de genetique vol. 35 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.