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	301.	Duplication in the long arm of the X-chromosome associated with spastic paraparesis and premature menopause. [electronic resource] by Kleczkowska, A Fryns, J P Van den Berghe, H Producer: 19940203 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	302.	Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant. [electronic resource] by Lukusa, T Devriendt, K Holvoet, M Fryns, J P Producer: 20000519 In: American journal of medical genetics vol. 91 Availability: No items available. Save to lists Add to cart (remove)
	303.	Distinct familial syndrome of severe to profound mental retardation, spastic paraplegia with contrasting axial hypotonia, short stature and distinct craniofacial appearance with nasal hypoplasia. [electronic resource] by Fryns, J P Devriendt, K Detroch, C Decock, P Producer: 19980710 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	304.	Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother. [electronic resource] by Fryns, J P Smeets, E Devriendt, K Petit, P Producer: 19980917 In: Annales de genetique vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	305.	Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotype. [electronic resource] by Goossens, E Decock, P Potgieter, S Fryns, J P Producer: 19991227 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	306.	Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age. [electronic resource] by Swillen, A Devriendt, K Ghesquière, P Fryns, J P Producer: 20020723 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	307.	MURCS association with duplicated thumb. [electronic resource] by López, A G-M Fryns, J-P Devriendt, K Producer: 20030207 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	308.	Diaphragmatic hernia with extralobar lung sequestration in the Beckwith-Wiedemann syndrome. [electronic resource] by Witters, L Moerman, Ph Brouwers, A Fryns, J P Producer: 20050111 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	309.	Multiple circumferential skin creases: another sign of genetic mosaicism? [electronic resource] by Devriendt, Koen Fryns, J P Vanhole, C Bogaert, G Producer: 20050505 In: American journal of medical genetics. Part A vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	310.	Down's syndrome in brother and sister without evident trisomy 21. [electronic resource] by Parloir, C Fryns, J P Van den Berghe, H Producer: 19800215 In: Human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	311.	Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome. [electronic resource] by Borghgraef, M Fryns, J P Van Den Berghe, H Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	312.	Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetus. [electronic resource] by Petit, P Thomas, D Moerman, P Fryns, J P Producer: 19910724 In: European journal of obstetrics, gynecology, and reproductive biology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	313.	Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity? [electronic resource] by Fryns, J P Vogels, A van den Berghe, H Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	314.	Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum. [electronic resource] by Fryns, J P Chrzanowska, K Van den Berghe, H Producer: 19891003 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	315.	Familial transmission of autosomal whole arm translocation. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19890502 In: Journal of medical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	316.	Paracentric inversions in man. [electronic resource] by Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19860917 In: Human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	317.	A longitudinal study of intelligence in Dutch fragile X boys. [electronic resource] by Wiegers, A M Curfs, L M Fryns, J P Producer: 19931217 In: Birth defects original article series vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	318.	Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entity. [electronic resource] by Parloir, C Fryns, J P Van den Berghe, H Producer: 19790925 In: Human genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	319.	Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child. [electronic resource] by Soekarman, D Fryns, J P van den Berghe, H Producer: 19930201 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	320.	Y to X translocation in man. [electronic resource] by van den Berghe, H Petit, P Fryns, J P Producer: 19770630 In: Human genetics vol. 36 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.