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	161.	Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis). [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19880302 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)
	162.	Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations. [electronic resource] by Petit, P Moerman, P Fryns, J P Producer: 19920610 In: Clinical genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Smith-Lemli-Opitz syndrome: the changing phenotype with age. [electronic resource] by de Die-Smulders, C Fryns, J P Producer: 19920910 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	164.	Pre- and postnatal growth retardation with severe mental retardation, acral limb deficiencies and ocular anomalies: a new syndrome of inherited intrauterine dwarfism? [electronic resource] by Fryns, J P van den Berghe, H Producer: 19780628 In: Acta paediatrica Belgica vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	165.	Severe limb malformations in 4p deletion. [electronic resource] by Haspeslagh, M Fryns, J P Moerman, P Producer: 19840608 In: Clinical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	Apparently enhanced visual information processing in female fragile X carriers: preliminary findings. [electronic resource] by Steyaert, J Borghgraef, M Fryns, J P Producer: 19941116 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)). [electronic resource] by Vogels, A Haegeman, J Fryns, J P Producer: 19980108 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	168.	Diaphragmatic hernia in the Coffin-Siris syndrome. [electronic resource] by Delvaux, V Moerman, P Fryns, J P Producer: 19980710 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	169.	Moderate mental retardation without dysmorphic symptoms in intrachromosomal 11p12 duplication. [electronic resource] by Goossens, E Cayenberghs, R Fryns, J P Producer: 19991227 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	170.	Vocal cord paralysis and cystic kidney disease in Hajdu-Cheney syndrome. [electronic resource] by Fryns, J P Stinckens, C Feenstra, L Producer: 19970723 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	Rieger syndrome and interstitial 4q26 deletion. [electronic resource] by Fryns, J P Van Den Berghe, H Producer: 19921125 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	172.	Lobar holoprosencephaly and Xq22 deletion. [electronic resource] by Petit, P Moerman, P Fryns, J P Producer: 19920313 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	173.	The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter). [electronic resource] by Petit, P Moerman, P Fryns, J P Producer: 19920424 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	174.	Familial paracentric inversion of the short arm of chromosome 3. [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)
	175.	"Adult" form of polycystic kidney disease in neonates. [electronic resource] by Fryns, J P Van Den Berghe, H Producer: 19790426 In: Clinical genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	176.	Acrofacial dysostosis with postaxial limb deficiency. [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19880406 In: American journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	[Prune belly syndrome, a secondary urethral functional obstruction due to prostatic hypoplasia]. [electronic resource] by Moerman, P Fryns, J P Goodeeris, P Producer: 19840817 In: Journal de genetique humaine vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	178.	Paracentric Inversion in man: personal experience and review of the literature. [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19801024 In: Human genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	The Cohen syndrome. [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19820412 In: Journal de genetique humaine vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	180.	Normal testicular histology in a mid-trimester 49,XXXXY fetus. [electronic resource] by Fryns, J P Moerman, P Kleczkowska, A Producer: 19951120 In: Clinical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.