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	461.	Unusual in vivo rearrangements of the Y chromosome with mitotic instability in vitro. [electronic resource] by Fryns, J P Cassiman, J J Van den Berghe, H Producer: 19790313 In: Human genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	Distal 10p deletion syndrome. [electronic resource] by Fryns, J P De Muelenaere, A Van den Berghe, H Producer: 19811122 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	463.	Partial distal 12q trisomy. [electronic resource] by de Muelenaere, A Fryns, J P Van Den Berghe, H Producer: 19810613 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	464.	Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay: a 4p deletion? [electronic resource] by de Die-Smulders, C Schrander-Stumpel, C Fryns, J P Producer: 19940204 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	465.	Spectrum of clinical and autopsy findings in trisomy 18 syndrome. [electronic resource] by Moerman, P Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19821221 In: Journal de genetique humaine vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	466.	Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis. [electronic resource] by Lukusa, T Smeets, E Vermeesch, J R Fryns, J P Producer: 20030425 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	467.	Björnstad syndrome in a patient with mental retardation. [electronic resource] by Van Buggenhout, G Trommelen, J Hamel, B Fryns, J P Producer: 19981202 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	468.	Prenatal diagnosis and genetic counseling in 21 trisomy: its impact on family planning. [electronic resource] by Evers-Keibooms, G Fryns, J P ven den Berghe, H Producer: 19811118 In: Journal de genetique humaine vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	469.	Mosaic supernumerary small ring chromosome. [electronic resource] by Fryns, J P van Herck, G van den Berghe, H Producer: 19820412 In: Journal de genetique humaine vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	470.	Cowden syndrome: report of a large family with macrocephaly and increased severity of signs in subsequent generations. [electronic resource] by Hanssen, A M Werquin, H Suys, E Fryns, J P Producer: 19940419 In: Clinical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	471.	The oculo-dento-digital syndrome: male-to-male transmission and variable expression in a family. [electronic resource] by Ioan, D M Dumitriu, L Belengeariu, V Fryns, J P Producer: 19970819 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	472.	Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences. [electronic resource] by Vermeesch, J R Baten, E Fryns, J-P Devriendt, K Producer: 20030430 In: Clinical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	473.	"A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities": Cohen syndrome with thrombocytopenia. [electronic resource] by De Ravel, T J L Dillen, K Fryns, J P Producer: 20030425 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	474.	Segmentary fibrous dysplasia manifesting as macrodactyly. [electronic resource] by Keymolen, K De Smet, L Kenis, H Fryns, J P Producer: 20000127 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	475.	FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish. [electronic resource] by Balikova, I Devriendt, K Fryns, J-P Vermeesch, J R Publication details: Molecular syndromology 2010 In: Molecular syndromology vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	476.	X-linked recessively inherited non-specific mental retardation. Report of a large family. [electronic resource] by Deroover, J Fryns, J P Parloir, C Van den Berghe, H Producer: 19780517 In: Annales de genetique vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	477.	Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter). [electronic resource] by Fryns, J P Deroover, J Haegeman, J Van den Berghe, H Producer: 19790725 In: Human genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	478.	Moderate mental retardation and nonspecific dysmorphic syndrome associated with ring chromosome 9. [electronic resource] by Fryns, J P Lambrechts, A Jansseune, H 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)
	479.	Adults with Williams syndrome. [electronic resource] by Fryns, J P Borghgraef, M Volcke, P Van den Berghe, H Producer: 19911024 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)
	480.	Noonan phenotype in the basal cell nevus syndrome. [electronic resource] by Grubben, C Fryns, J P Smeets, E Van den Berghe, H Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.