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	281.	Penile enlargement in tetrasomy 18p: an additional feature? [electronic resource] by Fryns, J P Grubben, C Van Den Berghe, H Producer: 19910705 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	282.	[Chromosome X-linked mental retardation and marfanoid syndrome]. [electronic resource] by Fryns, J P Buttiens, M van den Berghe, H Producer: 19880725 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	283.	X-chromosome polysomy in the male. The Leuven experience 1966-1987. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19881019 In: Human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	284.	Pericentric inversions in man: personal experience and review of the literature. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19870605 In: Human genetics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	285.	Distal deletion of the long arm of chromosome 6: a specific phenotype? [electronic resource] by Fryns, J P Bettens, W Van den Berghe, H Producer: 19860530 In: American journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	286.	Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome? [electronic resource] by Legius, E Fryns, J P Van den Berghe, H Producer: 19891003 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	287.	X-to-X translocation associated with gonadal dysgenesis and discrete Turner syndrome stigmata; a case report. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19891113 In: European journal of obstetrics, gynecology, and reproductive biology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	288.	An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation. [electronic resource] by Buttiens, M Fryns, J P van den Berghe, H Producer: 19900119 In: Clinical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	289.	Trisomy of the short arm of chromosome 4: the changing phenotype with age. [electronic resource] by Kleczkowska, A Fryns, J P van den Berghe, H Producer: 19930422 In: Annales de genetique vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	290.	The role of the Y-chromosome in sex determination. [electronic resource] by Lukusa, T Fryns, J P van der Berghe, H Producer: 19920701 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	291.	Complex chromosomal rearrangements (CCR) and their genetic consequences. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19830311 In: Journal de genetique humaine vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	292.	Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl. [electronic resource] by Fryns, J P Verresen, H Van den Berghe, H Producer: 19750421 In: Humangenetik vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	293.	Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells. [electronic resource] by Van den Berghe, H Fryns, J P Verresen, H Producer: 19730308 In: Journal of medical genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	294.	Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defect. [electronic resource] by Petit, P Moerman, P Legius, E Fryns, J P Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	295.	The Coffin syndrome. [electronic resource] by Fryns, J P Vinken, L Van den Berghe, H Producer: 19770622 In: Human genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	296.	Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadism. [electronic resource] by Devriendt, K Van den Berghe, H Fryns, J P Producer: 19961024 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	297.	Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome? [electronic resource] by de Die-Smulders, C Vles, H Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	298.	Frontonasal malformation and reciprocal translocation t(15;22)(q22;q13) [electronic resource] by Fryns, J P Kleczkowska, A van den Berghe, H Producer: 19931104 In: Clinical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	299.	A familial syndrome of dwarfism, bilateral club feet, premature aging and progressive panhypogammaglobulinemia. [electronic resource] by Lenaerts, J Fryns, J P Westhovens, R Dequeker, J Producer: 19940919 In: The Journal of rheumatology vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	300.	A distinct multiple congenital anomalies syndrome associated with distal 5q deletion (q35.1qter). [electronic resource] by Kleczkowska, A Fryns, J P van den Berghe, H Producer: 19931116 In: Annales de genetique vol. 36 Availability: No items available. Save to lists Add to cart (remove)

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