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	481.	Turner syndrome: the Leuven experience (1965-1989) in 478 patients. I. Patient's age at the time of diagnosis in relation to chromosomal findings. [electronic resource] by Kleczkowska, A Kubien, E Fryns, J P Van den Berghe, H Producer: 19910801 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	482.	Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome. [electronic resource] by Soekarman, D Fryns, J P Casaer, P Van Den Berghe, H Producer: 19920424 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	483.	On the recurrence risk of 18 trisomy. [electronic resource] by Ristić, O Fryns, J P Kleczowska, A Van Den Berghe, H Producer: 19911204 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	484.	[Sexual ambiguity and non-fluorescent Y chromosome in 45,X/46,XY mosaicism]. [electronic resource] by Lukusa, T Fryns, J P Vereecken, R Van den Berghe, H Producer: 19861120 In: Archives francaises de pediatrie vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	485.	[Sexual ambiguity and a non-fluorescent Y chromosome]. [electronic resource] by Fryns, J P Lukusa, T Vereecken, R Van den Berghe, H Producer: 19870828 In: Journal de genetique humaine vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	486.	Excess of mental retardation and/or congenital malformation in reciprocal translocations in man. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Van den Berghe, H Producer: 19860305 In: Human genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	487.	Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenita. [electronic resource] by Moerman, P Fryns, J P Van Dijck, H Lauweryns, J M Producer: 19851218 In: Virchows Archiv. A, Pathological anatomy and histopathology vol. 408 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	488.	Schinzel acrocallosal syndrome: a variant example of the Greig syndrome? [electronic resource] by Legius, E Fryns, J P Casaer, P Boel, M Eggermont, E Producer: 19860424 In: Annales de genetique vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	489.	Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal. [electronic resource] by Fryns, J P Kleczkowska, A Casaer, P van den Berghe, H Producer: 19860701 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	490.	Severe midline fusion defects in a newborn with 10q26----qter deletion. [electronic resource] by Fryns, J P Kleczkowska, A Fivez, H Van den Berghe, H Producer: 19890901 In: Annales de genetique vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	491.	Tuberous sclerosis. Bourneville disease. [electronic resource] by Fryns, J P Parloir, C Deroover, J Van den Berghe, H Producer: 19780828 In: Acta paediatrica Belgica vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	492.	Cystic hygroma and multiple pterygium syndrome. [electronic resource] by Fryns, J P Vandenberghe, K Moerman, P van den Berghe, H Producer: 19850320 In: Annales de genetique vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	493.	Klinefelter syndrome and two fragile X chromosomes. [electronic resource] by Fryns, J P Kleczkowska, A Wolfs, I van den Berghe, H Producer: 19850114 In: Clinical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	494.	Cytogenetic findings in moderate and severe mental retardation. A study of an institutionalized population of 1991 patients. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Van den Berghe, H Producer: 19850410 In: Acta paediatrica Scandinavica. Supplement vol. 313 Availability: No items available. Save to lists Add to cart (remove)
	495.	Myotonic dystrophy and autosomal balanced translocation t(2;20)(p21;q11). [electronic resource] by Fryns, J P Kleczkowska, A Bulcke, I van den Berghe, H Producer: 19840709 In: Clinical genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	496.	Fertility in patients with X chromosome deletions. [electronic resource] by Fryns, J P Kleczkowska, A Petit, P van den Berghe, H Producer: 19830214 In: Clinical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	497.	Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3). [electronic resource] by Kleczkowska, A Decock, P van den Berghe, H Fryns, J P Producer: 19950420 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	498.	On two patients with and without the classical Wolf-Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndrome. [electronic resource] by Petit, P Schmit, J Van den Berghe, H Fryns, J P Producer: 19970213 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	499.	The Floating-Harbor syndrome: two affected siblings in a family. [electronic resource] by Fryns, J P Kleczkowska, A Timmermans, J van den Berghe, H 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)
	500.	MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication. [electronic resource] by Fryns, J P Borghgraef, M Lemmens, F van den Berghe, H Producer: 19940209 In: Clinical genetics vol. 44 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.