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	741.	The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling. [electronic resource] by Fryns, J P Curfs, L M Cassiman, J J van den Berghe, H Producer: 19930201 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	742.	Fryns syndrome: another example of non-lethal outcome with severe mental handicap. [electronic resource] by Hanssen, A M Schrander-Stumpel, C T Thiry, P A Fryns, J P Producer: 19930201 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	743.	Cognitive profile in adult, normal intelligent female fragile X carriers. [electronic resource] by Steyaert, J Borghgraef, M Gaulthier, C Fryns, J P Van den Berghe, H Producer: 19920716 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	744.	Cerebro-oculo-facio-skeletal (COFS) syndrome. The variability of presenting symptoms as a manifestation of two subtypes? [electronic resource] by Casteels, I Wijnants, A Casaer, P Eggermont, E Misotten, L Fryns, J P Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	745.	Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989. [electronic resource] by Kleczkowska, A Dmoch, E Kubien, E Fryns, J P Van den Berghe, H Producer: 19910801 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	746.	Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989. [electronic resource] by Kleczkowska, A Kubien, E Dmoch, E Fryns, J P Van den Berghe, H Producer: 19910801 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	747.	Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype. [electronic resource] by Fryns, J P Kleczkowska, A Kenis, H Decock, P Van den Berghe, H Producer: 19891201 In: Annales de genetique vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	748.	Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndrome. [electronic resource] by Fryns, J P Kleczkowska, A Lemmens, F Vandecasseye, W van den Berghe, H Producer: 19890814 In: Annales de genetique vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	749.	The pathology of trisomy 13 syndrome. A study of 12 cases. [electronic resource] by Moerman, P Fryns, J P van der Steen, K Kleczkowska, A Lauweryns, J Producer: 19890118 In: Human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	750.	Suggestively increased rate of infant death in children of fra(X) positive mothers. [electronic resource] by Fryns, J P Moerman, P Gilis, F d'Espallier, L Van den Berghe, H Producer: 19881108 In: American journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	751.	The fetal phenotype in 15q2 duplication. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, P Vandenberghe, K Van den Berghe, H Producer: 19880829 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	752.	Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3). [electronic resource] by Kleczkowska, A Fryns, J P Moerman, P Vandenberghe, K Van den Berghe, H Producer: 19871022 In: Clinical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	753.	Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33). [electronic resource] by Fryns, J P Smeets, E Eggermont, E Delire, C Van den Berghe, H Producer: 19790425 In: Acta paediatrica Belgica vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	754.	Inactivation pattern of the fragile X in heterozygous carriers. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Petit, P Van den Berghe, H Producer: 19840319 In: Human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	755.	Partial fra(X) phenotype with megalotestes in fra (X)-negative patients with acquired lesions of the central nervous system. [electronic resource] by Fryns, J P Dereymaeker, A Hoefnagels, M Volcke, P Van den Berghe, H Producer: 19860404 In: American journal of medical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	756.	Adults with Williams-Beuren syndrome: evaluation of the medical, psychological and behavioral aspects. [electronic resource] by Plissart, L Borghgraef, M Volcke, P Van den Berghe, H Fryns, J P Producer: 19950216 In: Clinical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	757.	Hereditary renal adysplasia: new observations and hypotheses. [electronic resource] by Moerman, P Fryns, J P Sastrowijoto, S H Vandenberghe, K Lauweryns, J M Producer: 19940922 In: Pediatric pathology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	758.	The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease. [electronic resource] by Devriendt, K Eyskens, B Swillen, A Dumoulin, M Gewillig, M Fryns, J P Producer: 19961211 In: European journal of pediatrics vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	759.	A specific phenotype associated with trisomy 15 mosaicism. [electronic resource] by Fryns, J P Kleczkowska, A Lagae, L Kenis, H van den Berghe, H Producer: 19931116 In: Annales de genetique vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	760.	Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation. [electronic resource] by Petit, P Devriendt, K Vermeesch, J R De Cock, P Fryns, J P Producer: 19980625 In: Annales de genetique vol. 41 Availability: No items available. Save to lists Add to cart (remove)

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