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	321.	X-X translocation in a patient with Turner's syndrome. [electronic resource] by Van den Berghe, H Fryns, J P Soyez, C Producer: 19740302 In: Humangenetik vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	322.	The various phenotypes in Xp deletion. observations in eleven patients. [electronic resource] by Fryns, J P Petit, P Van den Berghe, H Producer: 19811215 In: Human genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	323.	Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13). [electronic resource] by Petit, P 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)
	324.	Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation. [electronic resource] by Smeets, E Fryns, J P Van den Berghe, H Producer: 19941027 In: Clinical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	325.	Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene. [electronic resource] by Steyaert, J Borghgraef, M Legius, E Fryns, J P Producer: 19961213 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	326.	Nager acrofacial dysostosis. An adult male with severe neurological deficit. [electronic resource] by Fryns, J P Bonhomme, A Van den Berghe, H Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	327.	Progressive anterior vertebral body fusion, overgrowth and distinct craniofacial appearance. [electronic resource] by Fryns, J P Fabry, G Remans, J Colla, P Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	328.	Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31). [electronic resource] by Van Buggenhout, G Moerman, P H Fryns, J P Producer: 19970618 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	329.	Larsen syndrome presenting as a familial syndrome of dwarfism, distinct oldish facial appearance and bilateral clubfeet in mother and daughter. [electronic resource] by Fryns, J P Lenaerts, J Van den Berghe, H Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	330.	The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 children. [electronic resource] by Swillen, A Glorieux, N Peeters, M Fryns, J P Producer: 19960401 In: Clinical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	331.	Symmetrical tetraphocomelia without associated congenital malformations: a nosological dilemma. [electronic resource] by Witters, I Delattin, Ph Moerman, Ph Fryns, J-P Producer: 20030407 In: American journal of medical genetics vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	332.	Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation. [electronic resource] by Lukusa, T Devriendt, K Jaeken, J Fryns, J P Producer: 19990628 In: Clinical dysmorphology vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	333.	Second trimester miscarriage of a male fetus with incontinentia pigmenti. [electronic resource] by Devriendt, K Matthijs, G Fryns, J P Ballegeer, V Producer: 19990225 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	334.	Attitudes towards carrier testing in minors: a systematic review. [electronic resource] by Borry, P Fryns, J P Schotsmans, P Dierickx, K Producer: 20060404 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	335.	The long term evolution of 6 adult patients with Cohen syndrome and their behavioral characteristics. [electronic resource] by Peeters, K Willekens, D Steyaert, J Fryns, J P Producer: 20080926 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	336.	Twin reversed arterial perfusion sequence presenting as intrauterine cyst. [electronic resource] by Witters, I Coumans, A Willekes, C Fryns, J P Producer: 20140718 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	337.	Partial trisomy 22q with elevated arylsulfatase-A activity. [electronic resource] by Fryns, J P Jaeken, J van den Berghe, H Producer: 19800327 In: Annales de genetique vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	338.	Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation. [electronic resource] by Fryns, J P Delooz, J Van Den Berghe, H Producer: 19921113 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	339.	Partial duplication of the short arm of chromosome 9 (p13 leads to p22) in a child with typical 9p trisomy phenotype. [electronic resource] by Fryns, J P Casaer, P Van den Berghe, H Producer: 19790523 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	340.	Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11). [electronic resource] by Fryns, J P Casaer, P Van den Berghe, H Producer: 19790523 In: Human genetics vol. 46 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.