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	441.	Partial monosomy of the long arm of chromosome 16: a distinct clinical entity? [electronic resource] by Fryns, J P Bande-Knops, J Van Den Berghe, H Producer: 19790611 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	442.	Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlap. [electronic resource] by Moerman, P Fryns, J P Vandenberghe, K Lauweryns, J M Producer: 19920722 In: American journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	443.	A "new" epi-metaphyseal skeletal dysplasia in four members of a family. [electronic resource] by Fryns, J P De Bisschop, F Van den Berghe, H Producer: 19900410 In: Journal de genetique humaine vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	444.	Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome. [electronic resource] by Ioan, D M Maximilian, C Kleczkowska, A Fryns, J P Producer: 19930121 In: Annales de genetique vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	445.	The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family. [electronic resource] by Fryns, J P Van Noyen, G Van den Berghe, H Producer: 19810709 In: European journal of pediatrics vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	446.	Interstitial deletion of the long arm of chromosome 15. [electronic resource] by Fryns, J P de Muelenaere, A van den Berghe, H Producer: 19820708 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	447.	Primitive neuroectodermal tumor: a newly recognized cause of early fetal death. [electronic resource] by Moerman, P Goddeeris, P Fryns, J P Lauweryns, J M Producer: 19860410 In: Pediatric pathology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	448.	Kabuki (Niikawa-Kuroki) syndrome and paracentric inversion of the short arm of chromosome 4. [electronic resource] by Fryns, J P Van den Berghe, H Schrander-Stumpel, C Producer: 19950316 In: American journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	449.	X-linked mental retardation and neurological symptoms: a nosological approach. [electronic resource] by Schrander-Stumpel, C T Höweler, C J Fryns, J P Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	450.	Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14). [electronic resource] by Petit, P Hilliker, C Van Leuven, F 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)
	451.	Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient. [electronic resource] by Lukusa, T Van Buggenhout, G Devriendt, K Fryns, J P Producer: 20021129 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	452.	Early development of megarectum in myotonic dystrophy. [electronic resource] by Meijers, B Miserez, M Veerman-Wouters, G Fryns, J P Producer: 20020924 In: Clinical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	453.	The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism. [electronic resource] by Keymolen, K De Smet, L Bracke, P Fryns, J P Producer: 20000106 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	454.	Occipital Horn syndrome in a 2-year-old boy. [electronic resource] by De Paepe, A Loeys, B Devriendt, K Fryns, J P Producer: 19990922 In: Clinical dysmorphology vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	455.	Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7. [electronic resource] by Potgieter, S Matthijs, G De Cock, P Fryns, J P Producer: 20010215 In: European journal of pediatrics vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	456.	Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome? [electronic resource] by Vogels, A Lorenzetti, M E Gillis, P Fryns, J P Producer: 19970917 In: Annales de genetique vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	457.	Unilateral absence of the trapezius and pectoralis major muscle: a variant of Poland syndrome. [electronic resource] by Debeer, Ph Brys, P De Smet, L Fryns, J P Producer: 20030425 In: Genetic counseling (Geneva, Switzerland) vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	458.	Occipital scalp defect associated with valvular pulmonary stenosis. A new entity? [electronic resource] by Fryns, J P de Cock, P van den Berghe, H Producer: 19921202 In: Clinical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	459.	Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21)) [electronic resource] by Schrander-Stumpel, C T Fryns, J P Hamers, G G Producer: 19900516 In: Clinical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	460.	Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature. [electronic resource] by Schrander-Stumpel, C Schrander, J Fryns, J P Hamers, G Producer: 19900420 In: Clinical genetics vol. 37 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.