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	881.	Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3'/4 synpolydactyly. [electronic resource] by Debeer, P Schoenmakers, E F Thoelen, R Fryns, J P Van de Ven, W J Producer: 19981015 In: Cytogenetics and cell genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	882.	The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. [electronic resource] by Swillen, A Devriendt, K Legius, E Prinzie, P Vogels, A Ghesquière, P Fryns, J P Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	883.	MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies. [electronic resource] by Witters, I Devriendt, K Spinnewijn, D Moerman, P Van Assche, F A Fryns, J P Producer: 20020212 In: American journal of medical genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	884.	The Brachmann-de Lange syndrome in two siblings of normal parents. [electronic resource] by Fryns, J P Dereymaeker, A M Hoefnagels, M D'Hondt, F Mertens, G van den Berghe, H Producer: 19870930 In: Clinical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	885.	The Opitz hypertelorism-hypospadias syndrome. Further delineation of the spectrum of clinical findings. [electronic resource] by Dereymaeker, A M Fryns, J P Hoefnagels, M Heremans, G Marien, J Van den Berghe, H Producer: 19871120 In: Journal de genetique humaine vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	886.	Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosome. [electronic resource] by Zhang, J Marynen, P Devriendt, K Fryns, J P Van den Berghe, H Cassiman, J J Producer: 19891211 In: Human genetics vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	887.	Aniridia-Wilms' tumor association and 11p interstitial deletion. [electronic resource] by Fryns, J P Beirinckx, J De Sutter, E Derluyn, J Francois, J Van den Berghe, H Producer: 19810623 In: European journal of pediatrics vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	888.	Prenatal diagnosis of Meckel syndrome. [electronic resource] by Fryns, J P Vandenberghe, K Van Assche, F A Cassiman, J J van den Berghe, H Producer: 19810528 In: Journal de genetique humaine vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	889.	Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalities. [electronic resource] by Devriendt, K van den Oord, J De Vos, R Van den Berghe, H Fryns, J P Producer: 19960805 In: American journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	890.	Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association? [electronic resource] by Devriendt, K Naulaers, G Matthijs, G Van Houdt, K Devlieger, H Gewillig, M Fryns, J P Producer: 19970610 In: Annales de genetique vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	891.	Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum. [electronic resource] by Schrander-Stumpel, C T De Groot-Wijnands, J B De Die-Smulders, C Fryns, J P Producer: 19940330 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	892.	Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli. [electronic resource] by Devriendt, K Jaeken, J Matthijs, G Van Esch, H Debeer, P Gewillig, M Fryns, J P Producer: 19990805 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	893.	De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia. [electronic resource] by Legius, E Wlodarska, I Selleri, L Evans, G A Wu, R Smet, G Fryns, J P Producer: 19961210 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	894.	Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome. [electronic resource] by Witters, I Moerman, P Louwagie, D Van Assche, F A Migeon, B R Fryns, J P Producer: 20020221 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	895.	Ring chromosome 15 syndrome. Further delineation of the adult phenotype. [electronic resource] by Fryns, J P Kleczkowska, A Buttiens, M Jonckheere, P Brouckmans-Buttiens, K van den Berghe, H Producer: 19860701 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	896.	Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation. [electronic resource] by Kleczkowska, A Fryns, J P Buttiens, M de Bisschop, F Emmery, L Van den Berghe, H Producer: 19870414 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	897.	Autosomal dominant isolated velopharyngeal insufficiency. [electronic resource] by Vantrappen, G Rommel, N Wellens, W Cremers, C W R J Fryns, J-P Devriendt, K Producer: 20020814 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	898.	Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13. [electronic resource] by Debeer, P Bacchelli, C Scambler, P J De Smet, L Fryns, J-P Goodman, F R Producer: 20021119 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	899.	Thymoma with a t(15;22)(p11;q11). [electronic resource] by Dal Cin, P De Wolf-Peeters, C Deneffe, G Fryns, J P Van den Berghe, H Producer: 19960830 In: Cancer genetics and cytogenetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	900.	Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years). [electronic resource] by Swillen, A Fryns, J P Kleczkowska, A Massa, G Vanderschueren-Lodeweyckx, M Van den Berghe, H Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.