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	201.	Further delineation of the KBG syndrome. [electronic resource] by Devriendt, K Holvoet, M Fryns, J P Producer: 19981202 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	202.	Preconception care. [electronic resource] by Witters, I Bogaerts, A Fryns, J P Producer: 20100903 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	203.	Possible excess of mental handicap and congenital malformations in autosomal reciprocal translocations. [electronic resource] by Fryns, J P van den Berghe, H Producer: 19800327 In: Annales de genetique vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	204.	The concurrence of Klinefelter syndrome and fragile X syndrome. [electronic resource] by Fryns, J P 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)
	205.	Inactivation pattern of the fragile X in heterozygous carriers. [electronic resource] by Fryns, J P 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)
	206.	Pre- and postnatal growth retardation--severe mental retardation--acral limb deficiencies with poorly keratinized nails. Another example of a distinct syndrome of inherited intrauterine dwarfism? [electronic resource] by Cartwright, J Nelson, M Fryns, J P Producer: 19920424 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	207.	Single central maxillary incisor and holoprosencephaly. [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19881207 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)
	208.	Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome. [electronic resource] by Petit, P Moerman, P Fryns, J P Producer: 19920323 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	209.	Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation--a new syndrome? [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19791121 In: European journal of pediatrics vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	210.	Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis. [electronic resource] by Fryns, J P Van Den Berghe, H Producer: 19790611 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	211.	Silver staining of the supernumerary chromosome in the cat-eye syndrome. [electronic resource] by Petit, P Godart, S Fryns, J P Producer: 19800926 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	212.	De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy. [electronic resource] by Fryns, J P Kleczkowska, A Kenis, H Producer: 19840612 In: Annales de genetique vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	213.	Partial duplication of the long arm of chromosome 4. [electronic resource] by Fryns, J P van den Berghe, H Producer: 19800530 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	214.	Translocation 46,X,t(Y;14)(q122;q111) in a case of sterility in the male. [electronic resource] by Petit, P Unglik, A Fryns, J P Producer: 19820708 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	215.	Trisomy of the short arm of chromosome number 9: a clinical entity. [electronic resource] by Fryns, J P van den Berghe, H Producer: 19801120 In: Acta paediatrica Belgica vol. Suppl 13 Availability: No items available. Save to lists Add to cart (remove)
	216.	Costello syndrome: the natural history of a true postnatal growth retardation syndrome. [electronic resource] by Umans, S Decock, P Fryns, J P Producer: 19951109 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	217.	Temperament in Williams syndrome. [electronic resource] by Plissart, L Borghgraef, M Fryns, J P Producer: 19960731 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	218.	On the nosology of the craniodigital syndromes: report of a family and review of the literature. [electronic resource] by Soekarman, D Volcke, P Fryns, J P Producer: 19980108 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	219.	Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies. [electronic resource] by Lukusa, T Moerman, P Fryns, J P Producer: 19970303 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	220.	Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene. [electronic resource] by Fryns, J P D'Hooghe, M Devriendt, K Producer: 19970303 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.