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	561.	Distinct facial appearance with nasal hypoplasia, constipation, severe mental retardation and hypotonia in two unrelated young males. [electronic resource] by Fryns, J P De Troch, C Van Mol, C Vandenbossche, L Producer: 19970326 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	562.	Marden-Walker phenotype: a diagnostic dilemma. [electronic resource] by Soekarman, D Volcke, P Legius, E Holvoet, M Fryns, J P Producer: 19960731 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	563.	Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome. [electronic resource] by Fryns, J P Devlieger, H Gewillig, M Lukusa, P Devriendt, K Producer: 19970303 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	564.	Early onset asymmetrical intrauterine growth retardation with fetal hypokinesia and variable expression of acral and genitourinary malformations: a new lethal MCA syndrome. [electronic resource] by Witters, I Moerman, P Van Assche, F A 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)
	565.	De novo interstitial tandem duplication of chromosome 20p12.1p13. [electronic resource] by de Ravel, T J L Vermeesch, J R Fryns, J-P Producer: 20030520 In: American journal of medical genetics. Part A vol. 117A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	566.	Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndrome. [electronic resource] by Schollen, E Smeets, E Deflem, E Fryns, J P Matthijs, G Producer: 20040220 In: Human mutation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	567.	Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entity. [electronic resource] by Keymolen, K Van Damme-Lombaerts, R Verloes, A Fryns, J P Producer: 20000710 In: American journal of medical genetics vol. 93 Availability: No items available. Save to lists Add to cart (remove)
	568.	Progressive pseudorheumatoid dysplasia: report of a patient with symptoms present at birth. [electronic resource] by van Buggenhout, G De Smet, L Maroteaux, P Fryns, J P Producer: 19990414 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	569.	Heterogeneity in omphalocoele with absent radial ray complex. [electronic resource] by Devriendt, K Fryns, J P Moerman, P Vanhole, C Devlieger, H Producer: 19990330 In: American journal of medical genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	570.	Triplication of distal chromosome 10q. [electronic resource] by Devriendt, K Matthijs, G Holvoet, M Schoenmakers, E Fryns, J P Producer: 19990611 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	571.	Prenatal diagnosis of schizencephaly after inhalation of organic solvents. [electronic resource] by Witters, I Cannie, M Casaer, P Devriendt, K Fryns, J-P Producer: 20080219 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	572.	The cardiofaciocutaneous syndrome: prenatal findings in two patients. [electronic resource] by Witters, I Denayer, E Brems, H Fryns, J P Legius, E Producer: 20080519 In: Prenatal diagnosis vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	573.	Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromes. [electronic resource] by Lukusa, T Fryns, J P Kleczkowska, A Van den Berghe, H Producer: 19920113 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	574.	Severe mental retardation in a patient with tricho-rhino-phalangeal syndrome type I and 8q deletion. [electronic resource] by Hamers, A Jongbloet, P Peeters, G Fryns, J P Geraedts, J Producer: 19900828 In: European journal of pediatrics vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	575.	On the familial occurrence of congenital bilateral absence of vas deferens. [electronic resource] by Kleczkowska, A Fryns, J P Steeno, O van den Berghe, H Producer: 19890616 In: Clinical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	576.	De novo Robertsonian D/D type translocations: the Leuven experience. [electronic resource] by Kleczkowska, A Fryns, J P Standaert, L van den Berghe, H Producer: 19891004 In: Clinical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	577.	Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation. [electronic resource] by Legius, E Moerman, P Fryns, J P Vandenberghe, K Eggermont, E Producer: 19890420 In: American journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	578.	Reciprocal translocations and full trisomy (trisomy 18 and trisomy 21) in the offspring. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, P Van den Berghe, H Producer: 19870619 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	579.	Unusual in vivo rearrangements of the Y-chromosome in two males. [electronic resource] by Fryns, J P Kleczkowska, A Lemmens, P Van den Berghe, H Producer: 19870619 In: Clinical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	580.	A new centromeric heteromorphism in the short arm of chromosome 20. [electronic resource] by Fryns, J P Kleczkowska, A Smeets, E van den Berghe, H Producer: 19881219 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)

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Your search returned 1120 results.