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	781.	Corpus callosum agenesis in two male infants of a heterozygotic triplet pregnancy. [electronic resource] by Vles, J S de Die-Smulders, C van der Hoeven, M Fryns, J P Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	782.	Interstitial telomeric sequences at the junction site of a jumping translocation. [electronic resource] by Vermeesch, J R Petit, P Speleman, F Devriendt, K Fryns, J P Marynen, P Producer: 19970708 In: Human genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	783.	Prenatal diagnosis of a terminal short arm deletion of chromosome 8 in a fetus with an atrioventricular septal defect. [electronic resource] by Devriendt, K Van Schoubroeck, D Eyskens, B Gewillig, M Vandenberghe, K Fryns, J P Producer: 19980319 In: Prenatal diagnosis vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	784.	Resolution of non-immune hydrops in Noonan syndrome with favorable outcome. [electronic resource] by Witters, I Spitz, B Van Hole, C Devriendt, K Fryns, J P Verbek, K Producer: 20021025 In: American journal of medical genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	785.	Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome. [electronic resource] by van Lieshout, C F De Meyer, R E Curfs, L M Fryns, J P Producer: 19981028 In: Journal of child psychology and psychiatry, and allied disciplines vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	786.	Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update. [electronic resource] by De Smedt, B Devriendt, K Fryns, J-P Vogels, A Gewillig, M Swillen, A Producer: 20071030 In: Journal of intellectual disability research : JIDR vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	787.	The Aarskog syndrome. [electronic resource] by Fryns, J P Macken, J Vinken, L Igodt-Ameye, L van den Berghe, H Producer: 19780915 In: Human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	788.	Pathogenesis of the lethal multiple pterygium syndrome. [electronic resource] by Moerman, P Fryns, J P Cornelis, A Bergmans, G Vandenberghe, K Lauweryns, J M Producer: 19900412 In: American journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	789.	The lethal multiple pterygium syndrome: prenatal ultrasonographic and postmortem findings; a case report. [electronic resource] by de Die-Smulders, C E Vonsée, H J Zandvoort, J A Fryns, J P Producer: 19900613 In: European journal of obstetrics, gynecology, and reproductive biology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	790.	A peculiar subphenotype in the fra(X) syndrome: extreme obesity-short stature-stubby hands and feet-diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome? [electronic resource] by Fryns, J P Haspeslagh, M Dereymaeker, A M Volcke, P Van den Berghe, H Producer: 19880328 In: Clinical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	791.	A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience. [electronic resource] by Schreppers-Tijdink, G A Curfs, L M Wiegers, A Kleczkowska, A Fryns, J P Producer: 19890309 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	792.	8p trisomy in a malformed foetus. [electronic resource] by Fryns, J P Petit, P Moerman, F Cassiman, J J van den Berghe, H Producer: 19821218 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	793.	Antenatal ultrasound diagnosis of fetal malformations: possibilities, limitations and dilemmas. [electronic resource] by Vandenberghe, K De Wolf, F Fryns, J P Eggermont, E Van den Berghe, H Producer: 19850409 In: European journal of obstetrics, gynecology, and reproductive biology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	794.	Prenatal diagnosis of campomelic dwarfism. [electronic resource] by Fryns, J P van den Berghe, K van Assche, A van den Berghe, H Producer: 19811122 In: Clinical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	795.	Split-hand/split-foot malformation with paternal mutation in the p63 gene. [electronic resource] by Witters, I Van Bokhoven, H Goossens, A Van Assche, F A Fryns, J P Producer: 20020412 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	796.	X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11. [electronic resource] by Strømme, P Sundet, K Mørk, C Cassiman, J J Fryns, J P Claes, S Producer: 19990824 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	797.	Encephalocraniocutaneous lipomatosis with a mutation in the NF1 gene. [electronic resource] by Legius, E Wu, R Eyssen, M Marynen, P Fryns, J P Cassiman, J J Producer: 19950918 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	798.	Non-immune hydrops fetalis caused by beta-glucuronidase deficiency (mucopolysaccharidosis VII). Study of a family with 3 affected siblings. [electronic resource] by Van Dorpe, J Moerman, P Pecceu, A Van den Steen, P Fryns, J P Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	799.	The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome. [electronic resource] by Van Esch, H Groenen, P Fryns, J P Van de Ven, W Devriendt, K Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	800.	Anogenital malformation with ambiguous genitalia as part of the OEIS complex. [electronic resource] by Witters, I Deprest, J Van Hole, C Hanssens, M Devlieger, H Fryns, J P Producer: 20050329 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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