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	581.	Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasias. [electronic resource] by Fryns, J P Hofkens, G Fabry, G van den Berghe, H Producer: 19880407 In: Clinical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	582.	[Structural chromosomal rearrangements in couples with repeated miscarriages. Experience in Louvain]. [electronic resource] by Fryns, J P Kleczkowska, A Kubien, E van den Berghe, H Producer: 19880725 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	583.	Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype. [electronic resource] by Fryns, J P Vinken, L Marien, J Van den Berghe, H Producer: 19790725 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	584.	The Noonan syndrome. [electronic resource] by Fryns, J P Van der Hauwaert, L Van den Berghe, H Producer: 19780426 In: Acta paediatrica Belgica vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	585.	The otopalatodigital syndrome. [electronic resource] by Fryns, J P Michielsen, P Vinken, L Van Den Berghe, H Producer: 19781220 In: Acta paediatrica Belgica vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	586.	Focal dermal hypoplasia (Goltz syndrome) in a male. [electronic resource] by Fryns, J P Dhondt, F Lindemans, L Van den Berghe, H Producer: 19780828 In: Acta paediatrica Belgica vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	587.	The 4p-syndrome, with a report of two new cases. [electronic resource] by Fryns, J P Eggermont, E Verresen, H Van den Berghe, H Producer: 19731025 In: Humangenetik vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	588.	Mosaic pericentric inversion of chromosome 2. [electronic resource] by Fryns, J P Petit, P Heffinck, R van den Berghe, H Producer: 19831220 In: Journal de genetique humaine vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	589.	New chromosomal syndromes. III. The 13q deletion syndrome. [electronic resource] by Fryns, J P Peeters, R Petit, P Van den Berghe, H Producer: 19811122 In: Acta paediatrica Belgica vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	590.	18p tetrasomy. Further evidence for a distinctive clinical syndrome. [electronic resource] by Fryns, J P Kleczkowska, A Marien, P Van den Berghe, H Producer: 19851008 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	591.	De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis. [electronic resource] by Fryns, J P Haspeslagh, M Agneessens, A van den Berghe, H Producer: 19850821 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	592.	Population cytogenetics of autosomal fragile sites. [electronic resource] by Petit, P Fryns, J P van den Berghe, H Hecht, F Producer: 19860506 In: Clinical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	593.	Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome. [electronic resource] by Fryns, J P Legius, E Demaerel, P van den Berghe, H Producer: 19970509 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	594.	Neuroblastoma and partial 15q duplication in the fetus. [electronic resource] by Fryns, J P Moerman, P Kleczkowska, A van den Berghe, H Producer: 19940720 In: Annales de genetique vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	595.	New findings in the behavioral profile of young FraX females. [electronic resource] by Borghgraef, M Umans, S Steyaert, J Legius, E Fryns, J P Producer: 19961213 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	596.	XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Van den Berghe, H Producer: 19960325 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	597.	Clinical follow up of a girl with "mental retardation with pterygia, shortness and distinct facial appearance" (Haspeslagh syndrome) [electronic resource] by Schrander-Stumpel, C T Pulles-Heintzberger, C F Fryns, J P Producer: 19951120 In: Clinical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	598.	Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome. [electronic resource] by Lukusa, T van den Berghe, L Smeets, E Fryns, J P Producer: 20000306 In: Annales de genetique vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	599.	Oto-onycho-peroneal syndrome: confirmation of a syndrome. [electronic resource] by Devriendt, K Stoffelen, D Pfeiffer, R Leys, A Fryns, J P Producer: 19980814 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)
	600.	X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms. [electronic resource] by Frints, S G M Froyen, G Marynen, P Fryns, J-P Producer: 20031104 In: Clinical genetics vol. 62 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.