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	341.	Ring chromosome 6: twenty years follow-up. [electronic resource] by Fryns, J P Kleczkowska, A van den Berghe, H Producer: 19910328 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	342.	Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndrome. [electronic resource] by Legius, E Fryns, J P Van den Berghe, H Producer: 19900726 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	343.	The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers. [electronic resource] by Borghgraef, M Fryns, J P van den Berghe, H Producer: 19900726 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	344.	Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndrome. [electronic resource] by Fryns, J P Vogels, A van den Berghe, H Producer: 19900420 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism. [electronic resource] by Fryns, J P Kleczkowska, A Van Den Berghe, H Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	346.	Moderate mental retardation and mild dysmorphic syndrome in proximal 7q interstitial deletion. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19871214 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	347.	[An excess of mental retardation and/or congenital malformations in carriers of reciprocal translocations. A difficult and delicate problem in genetic counseling]. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19870519 In: Journal de genetique humaine vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	348.	Multiple pterygium syndrome type Escobar in two brothers. Follow-up data from childhood to adulthood. [electronic resource] by Fryns, J P Volcke, P van den Berghe, H Producer: 19880929 In: European journal of pediatrics vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	349.	Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly. [electronic resource] by Schaap, C Schrander-Stumpel, C T Fryns, J P Producer: 19930201 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	350.	Small accessory chromosomes (SAC) and their genotype--phenotype correlation. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19830311 In: Journal de genetique humaine vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	351.	Robertsonian t(Dq;Dq) translocations in man. [electronic resource] by Fryns, J P Kleczkowska, A Van den Bergue, H Producer: 19821218 In: Journal de genetique humaine vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	352.	Phenotypic checklist to screen for fragile X syndrome in people with mental retardation. [electronic resource] by Maes, B Fryns, J P Ghesquière, P Borghgraef, M Producer: 20000802 In: Mental retardation vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	353.	Cenani-Lenz syndrome in father and daughter. [electronic resource] by De Smet, L De Beer, P Fryns, J P Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	354.	Chromosomal mosaicism limited to fibroblasts and MCA/MR syndrome with fetal hypokinesia of central nervous origin. [electronic resource] by Fryns, J P Legius, E Van den Berghe, H Producer: 19941230 In: Annales de genetique vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	355.	Isochromosome Xq in mosaicism with a cell line with two normal X-chromosomes: association with psychomotor retardation and neurological deficit. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19940328 In: Annales de genetique vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	356.	Prenatal growth retardation, microphthalmos/iris coloboma, cloudy cornea, urogenital anomalies and microcephaly. A possible new sublethal syndrome. [electronic resource] by Fryns, J P Verresen, H Van den Berghe, H Producer: 19970612 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	Severe axial mesodermal dysplasia spectrum in an infant of a diabetic mother. [electronic resource] by Depraetere, M Dehauwere, R Mariën, P Fryns, J P Producer: 19961017 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	358.	Hereditary hydronephrosis and the short arm of chromosome 6. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, P Vandenberghe, K Producer: 19930728 In: Human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	359.	Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family. [electronic resource] by Legius, E Schollen, E Matthijs, G Fryns, J P Producer: 19981110 In: European journal of human genetics : EJHG vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	A patient with Langer type of mesomelic dwarfism. [electronic resource] by Fryns, J P Mulier, F Van Den Berghe, H Producer: 19770224 In: Acta paediatrica Belgica vol. 29 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.