Your search returned 1120 results.

Results
	181.	Unusual 13/13 translocation and 13 trisomy phenotype. [electronic resource] by Fryns, J P Kleczkowska, A Kubien, E Producer: 19830407 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	182.	Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome. [electronic resource] by Devriendt, K D'Espallier, L Fryns, J P Producer: 19961010 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22)(q27;q121)) [electronic resource] by Fryns, J P Devriendt, K Moerman, P Producer: 19961217 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	184.	The KBG syndrome: follow-up data on three affected brothers. [electronic resource] by Soekarman, D Volcke, P Fryns, J P Producer: 19950302 In: Clinical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	Early urethral obstruction sequence and unbalanced translocation with terminal 10p duplication/1p deficiency. [electronic resource] by Fryns, J P Vandenberghe, K Deschrijver, D Producer: 19980326 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	186.	Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features. [electronic resource] by Smeets, E Vandenbossche, L Fryns, J P Producer: 20010726 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	187.	A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter). [electronic resource] by Lukusa, T Devriendt, K Fryns, J P Producer: 19990901 In: Annales de genetique vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	188.	Progeroid syndrome with facial teleangiectatic erythema, posterior subcapsular cataracts, calcification of basal ganglia and atrium septum defect type 2. [electronic resource] by Fryns, J P Dumoulin, M Hens, G Producer: 20000127 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	189.	On the association profound nerve deafness, semilobar holoprosencephaly, and minor midline developmental anomalies. [electronic resource] by Vantrappen, G Feenstra, L Fryns, J P Producer: 20000127 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	190.	A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism. [electronic resource] by Peeters, H Vermeesch, J Fryns, J P Producer: 20090330 In: Genetic counseling (Geneva, Switzerland) vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	191.	A follow-up study on 12 prenatally diagnosed boys with Klinefelter syndrome. [electronic resource] by Meeus, G Steyaert, J Fryns, J P Producer: 20060215 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	192.	Ocular symptoms in Cornelia de Lange syndrome. [electronic resource] by Evens, L Vinken, L Fryns, J P Producer: 19780628 In: Bulletin de la Societe belge d'ophtalmologie vol. 175 Availability: No items available. Save to lists Add to cart (remove)
	193.	Isochromosome Xq in Klinefelter syndrome. [electronic resource] by Fryns, J P Kleczkowska, A Steeno, O Producer: 19900808 In: American journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Patient with the combination of Klippel-Feil anomaly, partial agenesis of the sacrum, bladder incontinence, and unilateral hydronephrosis. [electronic resource] by Legius, E Fryns, J P Eggermont, E Producer: 19900606 In: Journal of craniofacial genetics and developmental biology vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	195.	X-linked mental retardation with Marfanoid habitus: a changing phenotype with age? [electronic resource] by Fryns, J P Van Den Berghe, H Producer: 19920421 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	196.	Transmission of fragile (X)(q27) from normal male(s). [electronic resource] by Fryns, J P van den Berghe, H Producer: 19830214 In: Human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	197.	Multiple diffuse hemangiomatosis. Case report and review of the literature. [electronic resource] by Fryns, J P Eggermont, E Eeckels, R Producer: 19750106 In: Zeitschrift fur Kinderheilkunde vol. 117 Availability: No items available. Save to lists Add to cart (remove)
	198.	Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriers. [electronic resource] by Fryns, J P Van den Berghe, H Producer: 19810521 In: Human genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	199.	Deletion in chromosome region 22q11 in a child with CHARGE association. [electronic resource] by Devriendt, K Swillen, A Fryns, J P Producer: 19980911 In: Clinical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	200.	Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcome. [electronic resource] by Petit, P Moerman, P Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1120 results.