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	421.	Hypomelanosis of Ito and severe sensorineural deafness. [electronic resource] by Fryns, J P Dereymaeker, A M Van Den Berghe, H Producer: 19921125 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	422.	A severe case of mandibuloacral dysplasia in a girl. [electronic resource] by Schrander-Stumpel, C Spaepen, A Fryns, J P Dumon, J Producer: 19920828 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	423.	Cenani-Lenz type of syndactyly: a complex type of syndactyly with multiple synostoses. [electronic resource] by De Smet, L Winnepenninckx, B Fryns, J P Fabry, G Producer: 19921125 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	424.	Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata. [electronic resource] by Fryns, J P De Waele, 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)
	425.	Caudal deficiency sequence in 7q terminal deletion. [electronic resource] by Schrander-Stumpel, C Schrander, J Fryns, J P Hamers, G Producer: 19881207 In: American journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	426.	Unusual translocation in Down syndrome. [electronic resource] by Fryns, J P de Waepenaert, E Van den Berghe, H Producer: 19801027 In: Acta paediatrica Belgica vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	427.	Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasia. [electronic resource] by Moerman, P Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19840502 In: Pediatrics vol. 73 Availability: No items available. Save to lists Add to cart (remove)
	428.	Nonimmunologic hydrops fetalis. A study of ten cases. [electronic resource] by Moerman, P Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19821216 In: Archives of pathology & laboratory medicine vol. 106 Availability: No items available. Save to lists Add to cart (remove)
	429.	Tertiary partial 14 trisomy 47, XX, plus 14q minus. [electronic resource] by Fryns, J P Cassiman, J J Van den Berghe, H Producer: 19750131 In: Humangenetik vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	430.	The Robinow syndrome. [electronic resource] by Petit, P Fryns, J P Goddeeris, P Perlmutter-Cremer, N Producer: 19810613 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	431.	Familial partial distal 18q (18q22-18q23) trisomy. [electronic resource] by De Muelenaere, A Fryns, J P Van den Berghe, H Producer: 19811122 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	432.	Cerebellar hypoplasia in a patient with velo-cardio-facial syndrome. [electronic resource] by Devriendt, K Thienen, M N Swillen, A Fryns, J P Producer: 19961127 In: Developmental medicine and child neurology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	433.	Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndrome. [electronic resource] by Ioan, D M Belengeanu, V Maximilian, C Fryns, J P Producer: 19931014 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	434.	Psychological consequences of presymptomatic testing for Huntington's disease. [electronic resource] by Evers-Kiebooms, G Decruyenaere, M Fryns, J P Demyttenaere, K Producer: 19970410 In: Lancet (London, England) vol. 349 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	435.	Kabuki make-up (Niikawa-Kuroki) syndrome in a girl presenting with vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism. [electronic resource] by Schrander-Stumpel, C Theunissen, P Hulsmans, R Fryns, J P Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	436.	Physical and psychomotor development of 1799 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype. [electronic resource] by Witters, I Moerman, P Van Assche, A Fryns, J-P Producer: 20030312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	437.	Distinct prenatal ultrasonographic cranial and cerebral findings in terminal deletion of the short arm of chromosome 1. [electronic resource] by Witters, I Vermeesch, J R Gyselaers, W Fryns, J P Producer: 20030211 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	438.	Sudden death in children with Prader-Willy syndrome: a call for collaboration. [electronic resource] by Schrander-Stumpel, C Sijstermans, H Curfs, L Fryns, J P Producer: 19981202 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	439.	Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene. [electronic resource] by Fryns, J P Willekens, D Van Schoubroeck, D Moerman, P Producer: 19981103 In: Clinical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	440.	The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation. [electronic resource] by Devriendt, K Holvoet, M De Mûelenaere, A Fryns, J P Producer: 20000428 In: Clinical genetics vol. 57 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.