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	401.	Fragile X mutation and FG syndrome-like phenotype. [electronic resource] by Piussan, C Mathieu, M Berquin, P 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)
	402.	Hyperacusis in Williams syndrome: a sample survey study. [electronic resource] by Van Borsel, J Curfs, L M Fryns, J P Producer: 19970819 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	403.	Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletion. [electronic resource] by Lukusa, T Devriendt, K Holvoet, M Fryns, J P Producer: 19981208 In: Clinical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	404.	Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications. [electronic resource] by Swillen, A Vogels, A Devriendt, K Fryns, J P Producer: 20010628 In: American journal of medical genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	405.	Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotype. [electronic resource] by Van Buggenhout, G De Coen, L Fryns, J P Producer: 19980917 In: Annales de genetique vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	406.	Dandy-Walker malformation in a male fetus with mosaic 45,X/46,X,del(Y)(q11). [electronic resource] by Witters, I Vandecruys, H Devlieger, R Fryns, J P Producer: 20090330 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	407.	Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophy. [electronic resource] by Moerman, P Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19830909 In: The Journal of pediatrics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	408.	The 4p-syndrome in a 24-year-old female. [electronic resource] by Fryns, J P de Muelenaere, A Van den Berghe, H Producer: 19820420 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	409.	Homozygosity by descent for a COL1A2 mutation in two sibs with severe osteogenesis imperfecta and mild clinical expression in the heterozygotes. [electronic resource] by De Paepe, A Nuytinck, L Raes, M Fryns, J P Producer: 19970512 In: Human genetics vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	410.	The Larsen syndrome. The diagnostic contribution of the analysis of the metacarpophalangeal pattern profile. [electronic resource] by De Smet, L Legius, E Fabry, G Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	411.	Holt-Oram syndrome: postaxial and central polydactyly as variable manifestations in a four generations family. [electronic resource] by Moens, P De Smet, L Fabry, G Fryns, J P Producer: 19940330 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	412.	Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult height. [electronic resource] by Legius, E Mulier, M Van Damme, B Fryns, J P Producer: 19940209 In: Clinical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	413.	Early urethral obstruction sequence and trisomy of the long arm of chromosome 1. [electronic resource] by van Buggenhout, G Cooreman, G Thienpont, L Fryns, J P Producer: 19951129 In: Annales de genetique vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	414.	Prenatal diagnosis of de novo distal 5q duplication associated with hygroma colli, fetal oedema and complex cardiopathy. [electronic resource] by Witters, I Van Buggenhout, G Moerman, P Fryns, J P Producer: 19990311 In: Prenatal diagnosis vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	415.	Mandibulo-acral dysplasia in a one-year-old boy. [electronic resource] by Vantrappen, G Feenstra, L Macours-Verelst, C Fryns, J P Producer: 20000512 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	416.	13q deletion syndrome in an adult mentally retarded patient. [electronic resource] by Van Buggenhout, G Trommelen, J Hamel, B Fryns, J P Producer: 19991227 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	417.	Cognitive and behavioral characteristics in 4 affected males of a family with non-specific X-linked mental retardation and TM4 SF2-gene mutation. [electronic resource] by De Vos, B Frints, S Borghgraef, M Fryns, J P Producer: 20030103 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	418.	Increased nuchal translucency with de novo acrocentric/18p translocation. [electronic resource] by Witters, I Delattin, Ph Van Schoubroeck, D Fryns, J P Producer: 20030103 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	419.	Facial asymmetry, cardiovascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome: a microdeletion/duplication in 13q. [electronic resource] by Maas, N Thienpont, B Vermeesch, J R Fryns, J P Producer: 20070508 In: Genetic counseling (Geneva, Switzerland) vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	420.	Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated. [electronic resource] by Chabchoub, E Willekens, D Vermeesch, J R Fryns, J-P Producer: 20130703 In: Clinical genetics vol. 81 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.