Your search returned 1120 results.

Results
	921.	Anomalous cerebral venous drainage in Aarskog syndrome. [electronic resource] by van den Bergh, P Fryns, J P Wilms, G Piot, R Dralands, G van den Bergh, R 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)
	922.	Two new cases of FMR1 deletion associated with mental impairment. [electronic resource] by Hirst, M Grewal, P Flannery, A Slatter, R Maher, E Barton, D Fryns, J P Davies, K Producer: 19950213 In: American journal of human genetics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	923.	The Prader-Willi syndrome: a self supporting program for children, youngsters and adults. [electronic resource] by Descheemaeker, M J Swillen, A Plissart, L Borghgraef, M Rasenberg, S Curfs, L M Fryns, J P Producer: 19941118 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	924.	Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor. [electronic resource] by de Ravel, T J Legius, E Brems, H Van Hoestenberghe, R Gillis, P H Fryns, J P Producer: 20020312 In: Clinical dysmorphology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	925.	Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11). [electronic resource] by Debeer, P Mols, R Huysmans, C Devriendt, K Van de Ven, W J M Fryns, J-P Producer: 20030430 In: Clinical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	926.	Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype. [electronic resource] by Witters, I Legius, E Devriendt, K Moerman, P Van Schoubroeck, D Van Assche, A Fryns, J P Producer: 20011018 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	927.	Mental retardation with pterygia, shortness and distinct facial appearance. A new MCA/MR syndrome. [electronic resource] by Haspeslagh, M Fryns, J P de Mûelenaere, A Schautteet, L van Eeckhoutte, I van den Berghe, H Producer: 19860219 In: Clinical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	928.	Distinct haematological disorder with deletion of long arm of no. 5 chromosome. [electronic resource] by Van den Berghe, H Cassiman, J J David, G Fryns, J P Michaux, J L Sokal, G Producer: 19750113 In: Nature vol. 251 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	929.	Problem behaviors and personality of children and adolescents with Prader-Willi syndrome. [electronic resource] by van Lieshout, C F de Meyer, R E Curfs, L M Koot, H M Fryns, J P Producer: 19980615 In: Journal of pediatric psychology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	930.	Prenatal findings in a monozygotic twin pregnancy with Costello syndrome. [electronic resource] by Van den Bosch, T Van Schoubroeck, D Fryns, J P Naulaers, G Inion, A M Devriendt, K Producer: 20020926 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	931.	Report of two Turkish infants with Norman-Roberts syndrome. [electronic resource] by Caksen, H Tuncer, O Kirimi, E Fryns, J P Uner, A Unal, O Cinal, A Odabaş, D Producer: 20040720 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	932.	A physical map of the chromosome 12 centromere. [electronic resource] by Vermeesch, J R Duhamel, H Raeymaekers, P Van Zand, K Verhasselt, P Fryns, J P Marynen, P Producer: 20040528 In: Cytogenetic and genome research vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	933.	A genetic-diagnostic survey in an institutionalized population of 173 severely mentally retarded patients. [electronic resource] by Fryns, J P Kleczkowska, A Dereymaeker, A Hoefnagels, M Heremans, G Marien, J van den Berghe, H Producer: 19870212 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	934.	Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS. [electronic resource] by Ruiz, J C Cuppens, H Legius, E Fryns, J P Glover, T Marynen, P Cassiman, J J Producer: 19951122 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)
	935.	Cohen syndrome: the clinical symptoms and stigmata at a young age. [electronic resource] by Fryns, J P Legius, E Devriendt, K Meire, F Standaert, L Baten, E Van den Berghe, H Producer: 19961203 In: Clinical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	936.	Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1q. [electronic resource] by Lukusa, T Van Buggenhout, G Devriendt, K Meireleire, J Van Goethem, G Roelen, L Fryns, J P Producer: 19990209 In: Annales de genetique vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	937.	Curcumin for the prevention of progression in monoclonal gammopathy of undetermined significance: A word of caution. [electronic resource] by Vermorken, A J M Zhu, J VAN DE Ven, W J M Cui, Y Fryns, J P Publication details: Experimental and therapeutic medicine Mar 2010 In: Experimental and therapeutic medicine vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	938.	Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype. [electronic resource] by Kleczkowska, A Fryns, J P Moerman, F Martens, M Eggermont, E Jaeken, J Van den Berghe, H Producer: 19890317 In: Helvetica paediatrica acta vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	939.	Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome? [electronic resource] by Verloes, A Gillerot, Y Delfortrie, J Zeevaert-Arnold, M T Collard, R Koulischer, L Fryns, J P Producer: 19910801 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	940.	X-linked neuropathy: gene localization with DNA probes. [electronic resource] by Fischbeck, K H ar-Rushdi, N Pericak-Vance, M Rozear, M Roses, A D Fryns, J P Producer: 19861229 In: Annals of neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1120 results.