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	861.	Macrocephaly and mental retardation. The unique association with short stature, spastic paraplegia and CNS malformations. [electronic resource] by Volcke, P Soekarman, D Vandenbussche, P Haegeman, J Smeets, E Thiry, P Fryns, J P Producer: 19930517 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	862.	Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome? [electronic resource] by Fryns, J P Smeets, E Thiry, P Geutjens, J Vinken, L Van den Berghe, H Producer: 19940527 In: American journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	863.	Lethal osteochondrodysplasia and de novo autosomal translocation involving the long arm of chromosome 4. [electronic resource] by Fryns, J P Legius, E Van den Berghe, H Moerman, P Vandenberghe, K Maroteaux, P Producer: 19941018 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	864.	Intelligence in individuals with a neurofibromatosis type 1 microdeletion. [electronic resource] by Descheemaeker, M J Roelandts, K De Raedt, T Brems, H Fryns, J P Legius, E Producer: 20050411 In: American journal of medical genetics. Part A vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	865.	Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedema. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, P van den Berghe, K van den Berghe, H Producer: 19880211 In: Annales de genetique vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	866.	Partial distal 6p trisomy in a malformed fetus. [electronic resource] by Fryns, J P Kleczkowska, A Moerman, F van den Berghe, K van den Berghe, H Producer: 19860701 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	867.	Opitz C syndrome and pseudohypoaldosteronism. [electronic resource] by De Koster, J Legius, E de Zegher, F Devlieger, H Fryns, J P Eggermont, E Producer: 19910125 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	868.	Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients. [electronic resource] by Chrzanowska, K H Fryns, J P Krajewska-Walasek, M Wisniewski, L Van den Berghe, H Producer: 19890627 In: Clinical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	869.	Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome. [electronic resource] by Chrzanowska, K H Fryns, J P Krajewska-Walasek, M Van den Berghe, H Wisniewski, L Producer: 19890927 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	870.	Caudal regression anomalad. [electronic resource] by Fryns, J P Haspeslagh, M Timmermans, J Hoedemaekers, G Goddeeris, P Van den Berghe, H Producer: 19820527 In: Acta paediatrica Belgica vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	871.	Perinatal mortality and XY/XX mosaicism. Report of two patients. [electronic resource] by Fryns, J P Haspeslagh, M Vandenbussche, E Goddeeris, P Eggermont, E Van den Berghe, H Producer: 19810327 In: Human genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	872.	Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35). [electronic resource] by Gu, X X Decorte, R Marynen, P Fryns, J P Cassiman, J J Raeymaekers, P Producer: 19961205 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	873.	Congenital pulmonary lymphangiectasis with chylothorax: a heterogeneous lymphatic vessel abnormality. [electronic resource] by Moerman, P Vandenberghe, K Devlieger, H Van Hole, C Fryns, J P Lauweryns, J M Producer: 19931007 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)
	874.	The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents. [electronic resource] by Vogels, A Devriendt, K Legius, E Decock, P Marien, J Hendrickx, G Fryns, J P Producer: 19990414 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	875.	Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1). [electronic resource] by Fryns, J P Kleczkowska, A Smeets, E Thiry, P Geutjens, J Van den Berghe, H Producer: 19910125 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	876.	Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein? [electronic resource] by Petit, P Bossens, M Thomas, D Moerman, P Fryns, J P Van den Berghe, H Producer: 19871022 In: Clinical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	877.	The foetal alcohol syndrome. [electronic resource] by Fryns, J P Deroover, J Parloir, C Goffaux, P Lebas, E Van Den Berghe, H Producer: 19770929 In: Acta paediatrica Belgica vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	878.	Ring chromosome 15 syndrome. [electronic resource] by Fryns, J P Jaeken, J Devlieger, H Debucquoy, P Eggermont, E Van den Berghe, H Producer: 19811025 In: Acta paediatrica Belgica vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	879.	Triploid-diploid mosaïcism in a deeply mentally retarded adult. [electronic resource] by Fryns, J P Vinken, L Geutjens, J Marien, J Deroover, J Van Den Berghe, H Producer: 19810613 In: Annales de genetique vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	880.	Prader-Willi-like phenotype in fragile X syndrome. [electronic resource] by Schrander-Stumpel, C Gerver, W J Meyer, H Engelen, J Mulder, H Fryns, J P Producer: 19940921 In: Clinical genetics vol. 45 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.