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	261.	Symbrachydactyly involving hands and feet. [electronic resource] by De Smet, L Fabry, G Fryns, J P Producer: 19980710 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	262.	Regional Proteus syndrome and somatic mosaicism. [electronic resource] by Smeets, E Fryns, J P Cohen, M M Producer: 19940808 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	263.	Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome. [electronic resource] by Fryns, J P Bonnet, D De Smet, L Producer: 19970318 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	264.	A new syndrome: multiple congenital abnormalities and mental retardation in two brothers. [electronic resource] by Dundar, M Ozdemir, S Y Fryns, J P Producer: 20120719 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	265.	Mental retardation with pterygia, shortness and distinct facial appearance. Confirmation of a new MCA/MR syndrome. [electronic resource] by Schrander-Stumpel, C Haspeslagh, M Fryns, J P Producer: 19890502 In: Clinical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	266.	Radial ray deficiency and ulnar ray deficiency in two sibs. [electronic resource] by De Smet, L Fabry, G Fryns, J P Producer: 19920910 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	267.	Hydrocephalus with features of VATER. [electronic resource] by Devriendt, K De Cock, P Fryns, J P Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	268.	Craniofrontonasal dysplasia: more severe expression in the mother than in her son. [electronic resource] by Devriendt, K Van Mol, C Fryns, J P Producer: 19961017 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	269.	Costello syndrome: report of an 8-month-old marasmic boy. [electronic resource] by Popa, M Ioan, D M Fryns, J P Producer: 19960731 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	270.	An unclassifiable type of spondylo-peripheral epiphyseal dysplasia associated with 21 trisomy. [electronic resource] by Ioan, D M Popa, M Fryns, J P Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	271.	MCA/MR syndrome with bilateral ablepharon of the upper eyelids, ambiguous genitalia, facial and skeletal anomalies. [electronic resource] by Ioan, D M Baloni, C Fryns, J P Producer: 20021129 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	272.	Terminal distal 13q trisomy due to de novo dup(13)(q32 --> qter). [electronic resource] by Ioan, D M Vermeesch, J Fryns, J P Producer: 20060404 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	273.	De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature. [electronic resource] by Lukusa, T Vermeesch, J R Fryns, J P Producer: 20050802 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	274.	The partial monosomy 10q syndrome: report on two patients and review of the developmental data. [electronic resource] by Schrander-Stumpel, C Fryns, J P Hamers, G Producer: 19911121 In: Journal of mental deficiency research vol. 35 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	275.	Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation. [electronic resource] by Frints, S G Moerman, P Fryns, J P Producer: 19970318 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	276.	Pre- and postnatal growth retardation, scaling skin, moderate mental retardation and quadrispasticity, hypospadias grade 2 and hydro-uretero nephrosis, postaxial polydactyly. A distinct MCA/MR syndrome? [electronic resource] by Fryns, J P Lagae, L Rizzo, W B Producer: 19990208 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	277.	Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father. [electronic resource] by Ioan, D M Dagomiz, D Fryns, J P Producer: 20030103 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	278.	Identification of a de novo 46, XY,4p+ with incomplete Wolf-Hirschhorn syndrome as 46,XY,der(4)t(4;8)(p16.3;p23.1) [electronic resource] by Petit, P Vermeersch, J R Fryns, J P Producer: 19980922 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	279.	The importance of excluding 13q deletion mosaicism in the diagnosis of retinoblastoma associated with dysmorphic features. [electronic resource] by Van Esch, H Aerssens, P Fryns, J P Producer: 20050802 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	280.	Prune-belly anomaly and large interstitial deletion of the long arm of chromosome 6. [electronic resource] by Fryns, J P Vandenberghe, K Van den Berghe, H Producer: 19920113 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.