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	541.	Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes. [electronic resource] by Stinckens, C Ensink, R Feenstra, L Fryns, J P Cremers, C Producer: 19970512 In: International journal of pediatric otorhinolaryngology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	542.	The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32. [electronic resource] by Kleczkowska, A Fryns, J P Lemay, P Van den Berghe, H Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	543.	Partial trisomy 3p/monosomy 9p with sex reversal. [electronic resource] by Witters, I Vermeesch, J R Moerman, P H Fryns, J P Producer: 20040823 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	544.	Macrocephaly, mental retardation, dysmorphism, and spastic paraplegia. [electronic resource] by de Ravel, T J L Van Driessche, J Fryns, J P Producer: 20050222 In: American journal of medical genetics. Part A vol. 127A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	545.	Abnormal first trimester screen in partial deletion of chromosome 6p21: a case-report. [electronic resource] by Hulsbergen, M H Van Calenbergh, S G K Fryns, J P Producer: 20071016 In: Genetic counseling (Geneva, Switzerland) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	546.	Ring chromosome 4 mosaicism and Potter sequence. [electronic resource] by Fryns, J P Kleczkowska, A Jaeken, J Van den Berghe, H Producer: 19880829 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	547.	Fertility and X-chromosome rearrangements: isodicentric X-chromosome formation in the mother and Xp deletion in her daughter. [electronic resource] by Fryns, J P Kleczkowska, A Debucquoy, P van den Berghe, H Producer: 19890413 In: Clinical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	548.	MASA syndrome: new clinical features and linkage analysis using DNA probes. [electronic resource] by Schrander-Stumpel, C Legius, E Fryns, J P Cassiman, J J Producer: 19910305 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	549.	Angelman's syndrome and 15q11-13 deletions. [electronic resource] by Fryns, J P Kleczkowska, A Decock, P Van den Berghe, H Producer: 19891003 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	550.	Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome? [electronic resource] by Delooz, J Moerman, P Van den Berghe, K Fryns, J P Producer: 19920910 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	551.	Inverted distal duplication of the long arm of chromosome 8: borderline intelligence and discrete dysmorphic syndrome. [electronic resource] by Kleczkowska, A Fryns, J P Decock, P Van den Berghe, H Producer: 19920313 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	552.	Transmission of ring chromosome 18 46,XX/46,XX,r(18) mosaicism in a mother and ring chromosome 18 syndrome in her son. [electronic resource] by Fryns, J P Kleczkowska, A Smeets, E Van Den Berghe, H Producer: 19921015 In: Annales de genetique vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	553.	Familial occurrence of severe ulnar aplasia and lobster claw feet: a new syndrome. [electronic resource] by van den Berghe, H Dequeker, J Fryns, J P David, G Producer: 19780724 In: Human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	554.	The psychological profile of the fragile X syndrome. [electronic resource] by Fryns, J P Jacobs, J Kleczkowska, A van den Berghe, H Producer: 19840521 In: Clinical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	555.	Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23. [electronic resource] by Fryns, J P Heremans, G Marien, J Van den Berghe, H Producer: 19831021 In: Human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	556.	Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys. [electronic resource] by Borghgraef, M Swillen, A Van den Berghe, H Fryns, J P Producer: 19951109 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	557.	Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q). [electronic resource] by Fryns, J P Eggermont, E Verresen, H van den Berghe, H Producer: 19740906 In: Humangenetik vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	558.	Opitz trigonocephaly syndrome and terminal transverse limb reduction defects. [electronic resource] by Fryns, J P Snoeck, L Kleczkowska, A Van den Berghe, H Producer: 19860428 In: Helvetica paediatrica acta vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	559.	Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery. [electronic resource] by Legius, E Hellemans, M Wilms, G Tillemans, B Fryns, J P Producer: 19940330 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	560.	Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndrome. [electronic resource] by Devriendt, K van den Berghe, K Moerman, P Fryns, J P Producer: 19961101 In: Prenatal diagnosis vol. 16 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.