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	621.	Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndrome. [electronic resource] by Verloes, A Gillerot, Y Langhendries, J P Fryns, J P Koulischer, L Producer: 19920803 In: American journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	622.	EEC syndrome without ectrodactyly: report of two new families. [electronic resource] by Fryns, J P Legius, E Dereymaeker, A M Van den Berghe, H Producer: 19900515 In: Journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	623.	The lethal multiple pterygium syndrome: a nosological approach. [electronic resource] by de Die-Smulders, C E Schrander-Stumpel, C T Fryns, J P Producer: 19901220 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	624.	The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome. [electronic resource] by Moerman, P Fryns, J P Vandenberghe, K Devlieger, H Lauweryns, J M Producer: 19890505 In: American journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	625.	Partial trisomy 14q due to familial t(14q-,11q+) translocation. [electronic resource] by Fryns, J P Van Eygen, M Tanghe, W Van Den Berghe, H Producer: 19770917 In: Human genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	626.	18q- syndrome in mother and daughter. [electronic resource] by Fryns, J P Logghe, N van Eygen, M van den Berghe, H Producer: 19790523 In: European journal of pediatrics vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	627.	Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn--karyotype: 46,XX,del(2)(q21;q24). [electronic resource] by Fryns, J P Van Bosstraeten, B Malbrain, H Van den Berghe, H Producer: 19780310 In: Human genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	628.	9p Trisomy/18p distal monosomy and multiple cutaneous leiomyomata. Another specific chromosomal site (18pter) in dominantly inherited multiple tumors? [electronic resource] by Fryns, J P Haspeslagh, M de Mûelenaere, A van Den Berghe, H Producer: 19850906 In: Human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	629.	Interstitial 16q deletion with typical dysmorphic syndrome. [electronic resource] by Fryns, J P Proesmans, W Van Hoey, G Van den Berghe, H Producer: 19820420 In: Annales de genetique vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	630.	Fragile-X syndrome and autism: a prevalent association or a misinterpreted connection? [electronic resource] by Maes, B Fryns, J P Van Walleghem, M Van den Berghe, H Producer: 19940330 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	631.	Goldston syndrome reconsidered. [electronic resource] by Moerman, P Pauwels, P Vandenberghe, K Lauweryns, J M Fryns, J P Producer: 19930928 In: Genetic counseling (Geneva, Switzerland) vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	632.	Neurofibromatosis type 1. [electronic resource] by Legius, E Descheemaeker, M J Fryns, J P Van den Berghe, H Producer: 19950209 In: Genetic counseling (Geneva, Switzerland) vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	633.	Cystic hygroma colli in triplo-X syndrome. [electronic resource] by Witters, I Moerman, P Jankelevitch, E Van Assche, A Fryns, J P Producer: 20000512 In: Genetic counseling (Geneva, Switzerland) vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	634.	Prenatal diagnosis of facial clefting as part of the oculo-auriculo-vertebral spectrum. [electronic resource] by Witters, I Schreurs, J Van Wing, J Wouters, W Fryns, J P Producer: 20010412 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	635.	Terminal 2q37 deletion and autistic behaviour. [electronic resource] by Lukusa, T Smeets, E Vogels, A Vermeesch, J R Fryns, J P Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	636.	A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genes. [electronic resource] by Caglayan, A O Lechno, S Gumus, H Bartsch, O Fryns, J P Producer: 20120306 In: Genetic counseling (Geneva, Switzerland) vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	637.	Congenital High Airway Obstruction Syndrome (CHAOS) as part of Fraser syndrome: ultrasound and autopsy findings. [electronic resource] by Mesens, T Witters, I Van Robaeys, J Peeters, H Fryns, J P Producer: 20140312 In: Genetic counseling (Geneva, Switzerland) vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	638.	Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome. [electronic resource] by Fryns, J P De Boeck, K Jaeken, J van den Berghe, H Producer: 19781202 In: Human genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	639.	Selective advantage of fra (X) heterozygotes. [electronic resource] by Vogel, F Crusio, W E Kovac, C Fryns, J P Freund, M Producer: 19910123 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	640.	The Meckel Syndrome. Pathological and cytogenetic observations in eight cases. [electronic resource] by Moerman, P Verbeken, E Fryns, J P Goddeeris, P Lauweryns, J M Producer: 19830623 In: Human genetics vol. 62 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.