Your search returned 1120 results.

Results
	601.	Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome. [electronic resource] by Vogels, A Matthijs, G Legius, E Devriendt, K Fryns, J-P Producer: 20030221 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	602.	The hand-foot-genital syndrome: on the variable expression in affected males. [electronic resource] by Fryns, J P Vogels, A Decock, P van den Berghe, H Producer: 19931021 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	603.	A young female with asymmetric manifestations of larsen syndrome: another example of unilateral somatic cell-line mosaicism. [electronic resource] by Frints, S G De Smet, L Fabry, G Fryns, J P Producer: 20010201 In: Clinical dysmorphology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	604.	Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third family. [electronic resource] by Debeer, Philippe Pykels, E Lammens, J Devriendt, K Fryns, J-P Producer: 20040130 In: American journal of medical genetics. Part A vol. 119A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	605.	Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome? [electronic resource] by Belengeanu, V Rozsnyai, K Farcaş, S Velea, I Fryns, J P Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	606.	Mental retardation, macrocephaly, short stature and craniofacial dysmorphism in three sisters. A new entity among the mental retardation-macrocephaly syndromes? [electronic resource] by Fryns, J P Dereymaeker, A M Haegeman, J van den Berghe, H Producer: 19880602 In: Clinical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	607.	Genetic control over fragile X chromosome expression. [electronic resource] by Hecht, F Fryns, J P Vlietinck, R F Van den Berghe, H Producer: 19860602 In: Clinical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	608.	Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son. [electronic resource] by Fryns, J P Kleczkowska, A Dereymaeker, A M Van den Berghe, H Producer: 19881123 In: Helvetica paediatrica acta vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	609.	A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy-Walker cyst. [electronic resource] by Moerman, P Vandenberghe, K Fryns, J P Haspeslagh, M Lauweryns, J M Producer: 19850429 In: Clinical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	610.	[Ring chromosome 6. Karotype 46, XY, r (6)-45, XY,-6]. [electronic resource] by Van den Berghe, H Fryns, J P Cassiman, J J David, G Producer: 19740928 In: Annales de genetique vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	611.	Fetal akinesia sequence caused by glycogenosis type VII. [electronic resource] by Moerman, P Lammens, M Fryns, J P Lemmens, F Lauweryns, J M Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	612.	Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region. [electronic resource] by Trottier, Y Imbert, G Poustka, A Fryns, J P Mandel, J L 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)
	613.	Association of hyperprolinaemia type I and heparin cofactor II deficiency with CATCH 22 syndrome: evidence for a contiguous gene syndrome locating the proline oxidase gene. [electronic resource] by Jaeken, J Goemans, N Fryns, J P François, I de Zegher, F Producer: 19961122 In: Journal of inherited metabolic disease vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	614.	Personality profiles of youngsters with Prader-Willi syndrome and youngsters attending regular schools. [electronic resource] by Curfs, L M Hoondert, V van Lieshout, C F Fryns, J P Producer: 19950921 In: Journal of intellectual disability research : JIDR vol. 39 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	615.	Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity. [electronic resource] by Devriendt, K Standaert, L Van Hole, C Devlieger, H Fryns, J P Producer: 19980326 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	616.	Diaphragmatic hernia as the first echographic sign in Apert syndrome. [electronic resource] by Witters, I Devriendt, K Moerman, P van Hole, C Fryns, J P Producer: 20000630 In: Prenatal diagnosis vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	617.	Cystic hygroma colli as the first echographic sign of the fetal akinesia sequence. [electronic resource] by Witters, I Moerman, P H Van Assche, F A Fryns, J P Producer: 20010726 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	618.	Preimplantation genetic diagnosis for an insertional translocation carrier. [electronic resource] by Melotte, C Debrock, S D'Hooghe, T Fryns, J P Vermeesch, J R Producer: 20050531 In: Human reproduction (Oxford, England) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	619.	Behavioural, academic and neuropsychological profile of normally gifted Neurofibromatosis type 1 children. [electronic resource] by Descheemaeker, M-J Ghesquière, P Symons, H Fryns, J P Legius, E Producer: 20050510 In: Journal of intellectual disability research : JIDR vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	620.	Pathogenesis of congenital cystic adenomatoid malformation of the lung. [electronic resource] by Moerman, P Fryns, J P Vandenberghe, K Devlieger, H Lauweryns, J M Producer: 19921125 In: Histopathology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1120 results.