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	701.	The variable clinical spectrum and mental prognosis of the acrocallosal syndrome. [electronic resource] by Fryns, J P Spaepen, A Grubben, C van den Berghe, H Casaer, P Producer: 19910723 In: Journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	702.	Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype. [electronic resource] by Kleczkowska, A Fryns, J P Moerman, P Vandenberghe, K Van den Berghe, H Producer: 19901205 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	703.	Thanatophoric dwarfism. [electronic resource] by Fryns, J P Moerman, P Devlieger, H Dewolf, F Van den Berghe, H Producer: 19790425 In: Acta paediatrica Belgica vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	704.	Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood. [electronic resource] by Kleczkowska, A Fryns, J P D'Hondt, F Jaeken, J Van den Berghe, H Producer: 19870925 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	705.	Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotype. [electronic resource] by Fryns, J P Vandenberghe, K Moerman, F Kleczkowska, A Van den Berghe, H Producer: 19870619 In: Clinical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	706.	Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns. [electronic resource] by Fryns, J P Kleczkowska, A Limbos, C Vandecasseye, W Van den Berghe, H Producer: 19860424 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	707.	Cytogenetic survey in couples with recurrent fetal wastage. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Petit, P Van den Berghe, H Producer: 19840319 In: Human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	708.	Prenatal ultrasound diagnosis of rhizomelic chondrodysplasia punctata in a primigravida. [electronic resource] by Sastrowijoto, S H Vandenberghe, K Moerman, P Lauweryns, J M Fryns, J P Producer: 19950112 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	709.	Confirmation of a new MR/male pseudohermaphroditism syndrome, Verloes type. [electronic resource] by de Die-Smulders, C van Schrojenstein Lantman-De Valk, H Fryns, J P Producer: 19940812 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	710.	VACTERL with hydrocephalus. A distinct entity with a variable spectrum of multiple congenital anomalies. [electronic resource] by Vandenborre, K Beemer, F Fryns, J P Vandenborne K [corrected to Vandenborre, K ] Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	711.	A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features. [electronic resource] by Wiegers, A M Curfs, L M Meijer, H Oostra, B Fryns, J P Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	712.	The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings. [electronic resource] by Lizcano-Gil, L A Garcia-Cruz, D Cantu, J M Fryns, J P Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	713.	The annual incidence of DiGeorge/velocardiofacial syndrome. [electronic resource] by Devriendt, K Fryns, J P Mortier, G van Thienen, M N Keymolen, K Producer: 19981110 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	714.	Behavioral phenotype in childhood type of dystrophia myotonica. [electronic resource] by Steyaert, J de Die-Smulders, C Fryns, J P Goossens, E Willekens, D Producer: 20001228 In: American journal of medical genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	715.	Unilateral symbrachydactyly of the foot. [electronic resource] by Mathijssen, I B Cossey, V Fryns, J P De Smet, L Devriendt, K Producer: 20061016 In: Genetic counseling (Geneva, Switzerland) vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	716.	Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differentiation from a complex cloacal malformation: a case report. [electronic resource] by Witters, I Meylaerts, L Peeters, H Coumans, A Wirjosoekarto, S Fryns, J-P Producer: 20130404 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	717.	Partial monosomy of the short arm of chromosome 9: a distinct clinical entity. [electronic resource] by Deroover, J Fryns, J P Parloir, C Haegeman, J van den Berghe, H Producer: 19790324 In: Human genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	718.	Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients. [electronic resource] by Borghgraef, M Fryns, J P Dielkens, A Pyck, K Van den Berghe, H Producer: 19871022 In: Clinical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	719.	Female pseudohermaphroditism with complete masculinisation of the external genitalia in two siblings. A new entity? [electronic resource] by Fryns, J P Kleczkowska, A Vandenberghe, K Haspeslagh, M Van den Berghe, H Producer: 19841009 In: European journal of pediatrics vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	720.	Complex chromosomal rearrangement in a mentally retarded boy without gross dysmorphic stigmata. [electronic resource] by Fryns, J P Kleczkowska, A Lebas, E Goffaux, P Van den Berghe, H Producer: 19840416 In: Acta paediatrica Scandinavica vol. 73 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.