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	501.	DiGeorge syndrome and unilateral symbrachydactyly. [electronic resource] by Devriendt, K De Smet, L De Boeck, K Fryns, J P Producer: 19980326 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	502.	Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes. [electronic resource] by Petit, P Devriendt, K Azou, M Gewillig, M Fryns, J P Producer: 19990414 In: Genetic counseling (Geneva, Switzerland) vol. 9 Availability: No items available. Save to lists Add to cart (remove)
	503.	Neuroblastoma in a mother and congenital central hypoventilation in her daughter: variable expression of the same genetic disorder? [electronic resource] by Devriendt, K Fryns, J P Naulaers, G Devlieger, H Alliet, P Producer: 20000324 In: American journal of medical genetics vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	504.	Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies. [electronic resource] by Thienpont, B Gewillig, M Fryns, J-P Devriendt, K Vermeesch, J Producer: 20060918 In: Cytogenetic and genome research vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	505.	Minimal dysmorphic stigmata in 9q deletion of paternal origin. [electronic resource] by Kleczkowska, A Fryns, J P Lemli, L Van den Berghe, H Producer: 19920701 In: Genetic counseling (Geneva, Switzerland) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	506.	On the excess of mental retardation and/or congenital malformations in apparently balanced reciprocal translocations. A critical review of the Leuven data 1966-1991. [electronic resource] by Fryns, J P Kleczkowska, A Kubień, E Van Den Berghe, H Producer: 19920421 In: Genetic counseling (Geneva, Switzerland) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	507.	[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"]. [electronic resource] by Fryns, J P Moerman, P Van den Berghe, H Aymé, S Producer: 19900410 In: Journal de genetique humaine vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	508.	Direct duplication 16q11.1----16q13 is not associated with a typical dysmorphic syndrome. [electronic resource] by Fryns, J P Kleczkowska, A Decock, P Van den Berghe, H Producer: 19900815 In: Annales de genetique vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	509.	Paracentric inversion in the short arm of chromosome 1. [electronic resource] by Deroover, J Fryns, J P Haegeman, J Van Den Bergh, H Producer: 19791024 In: Human genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	510.	Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21). [electronic resource] by Fryns, J P Melchoir, S Jaeken, J van den Berghe, H Producer: 19771229 In: Human genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	511.	Congenital bowing of the long bones. An example of a campomelic syndrome of the short-limbed normocephalic subtype. [electronic resource] by Fryns, J P Annicq, P Ulrix, M van den Berghe, H Producer: 19831220 In: Acta paediatrica Scandinavica vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	512.	Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents. [electronic resource] by Fryns, J P Kleczkowska, A Verresen, H van den Berghe, H Producer: 19831220 In: Clinical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	513.	Replication and inactivation of an isodicentric X: presence of an inactive centromere influences the replication patterns. [electronic resource] by Fryns, J P Petit, P Kleczkowska, A van den Berghe, H Producer: 19831220 In: Clinical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	514.	[Body and craniofacial biometric study of 26 Klinefelter patients compared to 307 controls]. [electronic resource] by Gueguen, A Tumba, A van den Berghe, H Fryns, J P Producer: 19831220 In: Journal de genetique humaine vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	515.	Effect of balanced X/autosome translocations on sexual and physical development. A personal experience in 4 patients. [electronic resource] by Kleczkowska, A Fryns, J P Vinken, L van den Berghe, H Producer: 19850429 In: Clinical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	516.	Complex chromosomal rearrangement (CCR), moderate mental retardation and discrete dysmorphic syndrome. [electronic resource] by Kleczkowska, A Fryns, J P Decock, P Van den Berghe, H Producer: 19940330 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	517.	Proteus syndrome and distal arthrogryposis. [electronic resource] by Ioan, D M Efimov, N Milcu, S M Fryns, J P Producer: 19980326 In: Genetic counseling (Geneva, Switzerland) vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	518.	Unexpected molecular findings in 2 previously described brothers with Smith-Lemli-Opitz syndrome. [electronic resource] by De Die-Smulders, C E Waterham, H R Fryns, J P Producer: 20000127 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	519.	Partial trisomy 9q syndrome with a de novo tandem duplication of 9q22.2-q31.1. [electronic resource] by Utine, G E Melotte, C Vermeesch, J R Fryns, J P Producer: 20060404 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	520.	A case of left isomerism with early fetal decompensation. [electronic resource] by Witters, I Debois, P Fryns, J P Devriendt, K Gewillig, M Producer: 20080415 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 30 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.