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	661.	Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder. [electronic resource] by Lukusa, T Vermeesch, J R Holvoet, M Fryns, J P Devriendt, K Producer: 20050111 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	662.	Distal arthrogryposis, specific facial dysmorphism and psychomotor retardation: a recognizable entity in surviving patients with the fetal akinesia deformation sequence. [electronic resource] by Schrander-Stumpel, C T Fryns, J P Schrander, J J Vles, J Producer: 19920313 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	663.	Lethal malformation syndrome in three siblings. A variable expression of the same entity? [electronic resource] by Van Regemorter, N Pierquin, G Vamos, E Elmer, C Fryns, J P Producer: 19920910 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	664.	Anterior basal encephalocele in the median cleft face syndrome. Comments on nosology and treatment. [electronic resource] by Grubben, C Fryns, J P De Zegher, F Van Den Berghe, H Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	665.	Congenital eventration of the diaphragm: an unusual cause of intractable neonatal respiratory distress with variable etiology. [electronic resource] by Moerman, P Fryns, J P Devlieger, H Van Assche, A Lauweryns, J Producer: 19870724 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	666.	Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21). [electronic resource] by Fryns, J P Logghe, N Van Eygen, M Van Der Berghe, H Producer: 19790917 In: Human genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	667.	New chromosomal syndromes. I. Partial trisomy of the distal portion of the long arm of chromosome number 10 (10q24 leads to 10qter): a clinical entity. [electronic resource] by Fryns, J P Logghe, N Van Eygen, M Van Den Berghe, H Producer: 19791227 In: Acta paediatrica Belgica vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	668.	Partial trisomy 18q in a newborn with typical 18 trisomy phenotype. [electronic resource] by Fryns, J P Detavernier, F van Fleteren, A van den Berghe, H Producer: 19790324 In: Human genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	669.	Partial trisomy for the long arm of chromosome 3 [3(q21 to qter)+] in a newborn with minor physical stigmata. [electronic resource] by Fryns, J P van Eygen, M Logghe, N Van den Berghe, H Producer: 19780508 In: Human genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	670.	Cardiovascular malformations in Turner's and Noonan's syndrome. [electronic resource] by Van der Hauwaert, L G Fryns, J P Dumoulin, M Logghe, N Producer: 19780828 In: British heart journal vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	671.	Cartilage-hair hypoplasia. [electronic resource] by Fryns, J P Pedersen, J C Pardon, W Van den Berghe, H Producer: 19811122 In: Acta paediatrica Belgica vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	672.	Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism. [electronic resource] by Fryns, J P Pedersen, J C Goddeeris, P van den Berghe, H Producer: 19800530 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	673.	Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood. [electronic resource] by Fryns, J P de Muelenaere, A Pedersen, J Van Den Berghe, H Producer: 19801218 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	674.	Melnick-Needles syndrome (osteodysplasty). Clinical and radiological heterogeneity. [electronic resource] by Dereymaeker, A M Christens, J Eeckels, R Heremans, G Fryns, J P Producer: 19870204 In: Helvetica paediatrica acta vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	675.	Calcification of cartilages, brachytelephalangy and peripheral pulmonary stenosis. Confirmation of the Keutel syndrome. [electronic resource] by Fryns, J P van Fleteren, A Mattelaer, P van den Berghe, H Producer: 19841025 In: European journal of pediatrics vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	676.	Association of Meckel syndrome with M-anisosplenia in one patient. [electronic resource] by Moerman, P Verbeken, E Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19830324 In: Clinical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	677.	Thrombocytopenia and cleft hand in monosomy 21. [electronic resource] by Vogels, A de Smet, L van den Berghe, H Fryns, J P Producer: 19940812 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	678.	Cognitive functioning and information processing of adult mentally retarded men with fragile-X syndrome. [electronic resource] by Maes, B Fryns, J P Van Walleghem, M Van den Berghe, H Producer: 19940718 In: American journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	679.	Adaptive behavior in the fragile X syndrome: profile and development. [electronic resource] by Wiegers, A M Curfs, L M Vermeer, E L Fryns, J P Producer: 19931123 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	680.	Identical psychological profile and behaviour pattern in different types of mutation in the FMR-1 region. [electronic resource] by Wiegers, A M DeVries, L B Curfs, L M 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)

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Your search returned 1120 results.