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	721.	Pierre-Robin anomalad, moderate mental retardation and distal 4q deletion. [electronic resource] by Fryns, J P Timmermans, J Hoedemaekers, J Emmery, L Van den Berghe, H Producer: 19811122 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	722.	Aberrant twinning (diprosopus) associated with anencephaly. [electronic resource] by Moerman, P Fryns, J P Goddeeris, P Lauweryns, J M Van Assche, A Producer: 19840107 In: Clinical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	723.	Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype. [electronic resource] by Fryns, J P Vogels, A Haegeman, J Eggermont, E van den Berghe, H Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	724.	Emotional and behavioral profile and child psychiatric diagnosis in the childhood type of myotonic dystrophy. [electronic resource] by Goossens, E Steyaert, J De Die-Smulders, C Willekens, D Fryns, J P Producer: 20010215 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	725.	Variable expression of the popliteal pterygium syndrome in two 3-generation families. [electronic resource] by Soekarman, D Cobben, J M Vogels, A Spauwen, P H Fryns, J P Producer: 19950906 In: Clinical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	726.	Megadolichosigmoid in a young male with Aarskog syndrome. [electronic resource] by Casteels, M Samain, H Penninckx, F Coremans, G Beirinckx, J Fryns, J P Producer: 19940812 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	727.	The 49,XXXXY syndrome. Clinical and psychological follow-up data. [electronic resource] by Borghgraef, M Fryns, J P Smeets, E Marien, J van Den Berghe, H Producer: 19881122 In: Clinical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	728.	[Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21]. [electronic resource] by Gilgenkrantz, S Fryns, J P Droulle, P Schweitzer, M Chadefaux, B Prieur, M Producer: 19870519 In: Journal de genetique humaine vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	729.	The 49,XXXXY syndrome: clinical and psychological findings in five patients. [electronic resource] by Curfs, L M Schreppers-Tijdink, G Wiegers, A Borghgraef, M Fryns, J P Producer: 19900912 In: Journal of mental deficiency research vol. 34 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	730.	Anodontia as the sole clinical sign of the ectrodactyly-ectodermal dysplasia-cleft lip (EEC) syndrome. [electronic resource] by Chranowska, K H Krajewska-Walasek, M Rump, Z Wisniewski, L Fryns, J P Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	731.	McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal period. [electronic resource] by Schaap, C de Die-Smulders, C E Kuijten, R H Fryns, J P Producer: 19920923 In: European journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	732.	Unusually long survival in a case of full triploidy of maternal origin. [electronic resource] by Fryns, J P van de Kerckhove, A Goddeeris, P van den Berghe, H Producer: 19771130 In: Human genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	733.	Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1. [electronic resource] by Fryns, J P Kleczkowska, A Buttiens, M Marien, P van den Berghe, H Producer: 19870212 In: Clinical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	734.	Cystic hygroma and hydrops fetalis in dup(11p) syndrome. [electronic resource] by Fryns, J P Kleczkowska, A Vandenberghe, K Moerman, F Van den Berghe, H Producer: 19851118 In: American journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	735.	Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome. [electronic resource] by Devriendt, K De Mars, K De Cock, P Gewillig, M Fryns, J P Producer: 19960625 In: Annales de genetique vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	736.	Apparently new "anophthalmia-plus" syndrome in sibs. [electronic resource] by Fryns, J P Legius, E Moerman, P Vandenberghe, K Van den Berghe, H Producer: 19960129 In: American journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	737.	Marden-Walker syndrome: case report, nosologic discussion and aspects of counseling. [electronic resource] by Garavelli, L Donadio, A Banchini, G Magnani, C Magnani, C Calzolari, E Fryns, J P Producer: 20001121 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	738.	Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32. [electronic resource] by Jamieson, C R Fryns, J P Jacobs, J Matthijs, G Abramowicz, M J Producer: 20010118 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	739.	Chromosome healing of constitutional chromosome deletions studied by microdissection. [electronic resource] by Vermeesch, J R Falzetti, D Van Buggenhout, G Fryns, J P Marynen, P Producer: 19981019 In: Cytogenetics and cell genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	740.	Partial trisomy 15q: report of a patient and literature review. [electronic resource] by Chandler, K Schrander-Stumpel, C T Engelen, J Theunissen, P Fryns, J P Producer: 19970819 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.