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	641.	Exclusively maternal transmission of autosomal dominant Brachmann-de Lange syndrome. [electronic resource] by de Die-Smulders, C Schrander-Stumpel, C Fryns, J P Theunissen, P Producer: 19950131 In: American journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	642.	Triple Test Screening for Down Syndrome: Looking Back on a False-Positive Result and Having or Not Having a Triple Test in Subsequent Pregnancies. [electronic resource] by Evers-Kiebooms, G Nys, K Decruyenaere, M Witters, I Fryns, J.-P Publication details: Community genetics Jul 2001 In: Community genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	643.	Increased frequency of chromosomal abnormalities in female partners of couples undergoing in vitro fertilization or intracytoplasmic sperm injection. [electronic resource] by Schreurs, A Legius, E Meuleman, C Fryns, J P D'Hooghe, T M Producer: 20000802 In: Fertility and sterility vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	644.	Terminal 6q25.3 deletion and abnormal behaviour. [electronic resource] by Lukusa, T Willekens, D Lukusa, N De Cock, F Fryns, J P Producer: 20020213 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	645.	Longitudinal changes in IQ among fragile X females: a preliminary multicenter analysis. [electronic resource] by Fisch, G S Simensen, R Arinami, T 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)
	646.	Neurofibromatosis type 1 in childhood: a study of the neuropsychological profile in 45 children. [electronic resource] by Legius, E Descheemaeker, M J Spaepen, A Casaer, P Fryns, J P Producer: 19940812 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	647.	Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p). [electronic resource] by Petit, P Devriendt, K Vermeesch, J R Meireleire, J Fryns, J P Producer: 19981202 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	648.	Proximal duplication of the long arm of chromosome 10 (10q11.2----10q22): a distinct clinical entity. [electronic resource] by Fryns, J P Kleczkowska, A Igodt-Ameye, L 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)
	649.	X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28. [electronic resource] by Fryns, J P Spaepen, A Cassiman, J J van den Berghe, H Producer: 19910913 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)
	650.	Association of distal arthrogryposis, mental retardation, whistling face, and Pierre Robin sequence: evidence for nosologic heterogeneity. [electronic resource] by Schrander-Stumpel, C Fryns, J P Beemer, F A Rive, F A Producer: 19910807 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	651.	On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men. [electronic resource] by Volcke, P Dereymaeker, A M Fryns, J P van den Berghe, H Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	652.	[49,XXXXX syndrome: apropos of a further case]. [electronic resource] by Tumba, A Fryns, J P van OOTEGHEM, G van den Berghe, H Producer: 19770520 In: L'union medicale du Canada vol. 106 Availability: No items available. Save to lists Add to cart (remove)
	653.	Langer-Giedion syndrome and deletion of the long arm of chromosome 8. [electronic resource] by Fryns, J P Logghe, N van Eygen, M Van den Berghe, H Producer: 19811221 In: Human genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	654.	Large congenital follicular ovarian cyst in a girl with Kabuki syndrome. [electronic resource] by Devriendt, K Van den Berghe, H Fryns, J P Van Reempst, P Producer: 19970207 In: American journal of medical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	655.	Lujan-Fryns syndrome in the differential diagnosis of schizophrenia. [electronic resource] by De Hert, M Steemans, D Theys, P Fryns, J P Peuskens, J Producer: 19961024 In: American journal of medical genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	656.	Micromelic dwarfism with cone epiphyses, metaphyseal dysplasia, and vertebral segmentation defects. [electronic resource] by Fryns, J P Lorenzetti, M E Maroteaux, P Van den Berghe, H Producer: 19960805 In: American journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	657.	Chromosome 22q11 deletion presenting as the Potter sequence. [electronic resource] by Devriendt, K Moerman, P Van Schoubroeck, D Vandenberghe, K Fryns, J P Producer: 19970716 In: Journal of medical genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	658.	Personal independence of adult mentally retarded men with fragile-X syndrome. [electronic resource] by Maes, B Fryns, J P Van Walleghem, M Van den Berghe, H Producer: 19941118 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	659.	PTEN mutation in a family with Cowden syndrome and autism. [electronic resource] by Goffin, A Hoefsloot, L H Bosgoed, E Swillen, A Fryns, J P Producer: 20010906 In: American journal of medical genetics vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	660.	Pre-academic and early academic achievement in children with velocardiofacial syndrome (del22q11.2) of borderline or normal intelligence. [electronic resource] by De Smedt, B Swillen, A Ghesquière, P Devriendt, K Fryns, J P Producer: 20030827 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.