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	981.	Vesico-ureteral reflux: a genetic condition? [electronic resource] by Devriendt, K Groenen, P Van Esch, H van Dijck, M Van de Ven, W Fryns, J P Proesmans, W Producer: 19980716 In: European journal of pediatrics vol. 157 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	982.	Familial deletions of chromosome 22q11: the Leuven experience. [electronic resource] by Swillen, A Devriendt, K Vantrappen, G Vogels, A Rommel, N Fryns, J P Eyskens, B Gewillig, M Dumoulin, M Producer: 19990310 In: American journal of medical genetics vol. 80 Availability: No items available. Save to lists Add to cart (remove)
	983.	A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidism. [electronic resource] by Akalin, I Senses, D A Ilgin-Ruhi, H Misirlioğlu, E Yalçiner, M Cetinkaya, E Fryns, J P Tükün, A Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	984.	A patient with a de novo 11q24.2-->qter deletion. [electronic resource] by Spruijt, L Fryns, J P Hanekom, J Engelen, J J Alofs, M Albrechts, J C Schrander-Stumpel, C T Producer: 20040720 In: Genetic counseling (Geneva, Switzerland) vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	985.	Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literature. [electronic resource] by Plomp, A S Schrander-Stumpel, C T Engelen, J J Sijstermans, J M Loneus, W H Fryns, J P Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	986.	5q- anomaly in a patient with disseminated teratoma. [electronic resource] by Tricot, G Fryns, J P Thomas, J Moerman, P Broeckaert-Van Orshoven, A Vermaelen, K Van Den Berghe, H Producer: 19830811 In: Cancer genetics and cytogenetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	987.	ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism. [electronic resource] by Van Esch, H Poirier, K de Zegher, F Holvoet, M Bienvenu, T Chelly, J Devriendt, K Fryns, J-P Producer: 20041202 In: Clinical genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	988.	Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience. [electronic resource] by Vantrappen, G Devriendt, K Swillen, A Rommel, N Vogels, A Eyskens, B Gewillig, M Feenstra, L Fryns, J P Producer: 19990804 In: Genetic counseling (Geneva, Switzerland) vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	989.	Linkage analysis in three families with nonspecific X-linked mental retardation. [electronic resource] by Claes, S Gu, X X Legius, E Lorenzetti, E Marynen, P Fryns, J P Cassiman, J J Raeymaekers, P Producer: 19961120 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	990.	Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients. [electronic resource] by Van Buggenhout, G J van Ravenswaaij-Arts, C Mieloo, H Syrrou, M Hamel, B Brunner, H Fryns, J P Producer: 20011204 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	991.	Novel syndromic form of X-linked complicated spastic paraplegia. [electronic resource] by Claes, S Devriendt, K Van Goethem, G Roelen, L Meireleire, J Raeymaekers, P Cassiman, J J Fryns, J P Producer: 20000927 In: American journal of medical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	992.	Psychotic disorders in Prader-Willi syndrome. [electronic resource] by Vogels, A De Hert, M Descheemaeker, M J Govers, V Devriendt, K Legius, E Prinzie, P Fryns, J P Producer: 20050222 In: American journal of medical genetics. Part A vol. 127A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	993.	Human homologues of Osr1 and Osr2 are not involved in a syndrome with distal limb deficiencies, oral abnormalities, and renal defects. [electronic resource] by Debeer, Ph de Ravel, T J L Devriendt, K Fryns, J-P Huysmans, C Van de Ven, W J M Producer: 20030210 In: American journal of medical genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	994.	Lateral facial clefts: a case report. [electronic resource] by de Die-Smulders, C E Moog, U Engelen, J J Peters, J J Damen, A Vos, W Fryns, J P Producer: 20020128 In: Genetic counseling (Geneva, Switzerland) vol. 12 Availability: No items available. Save to lists Add to cart (remove)
	995.	Lethal evolution of a newborn with consistent features of hydrolethalus syndrome--Romanian patient. [electronic resource] by Belengeanu, V Viskari, H Tallila, J Lahtela, J Farcas, S Andreescu, N Stoian, M Bohiltea, C L Fryns, J P Producer: 20111123 In: Genetic counseling (Geneva, Switzerland) vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	996.	Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia. [electronic resource] by Witters, I Legius, E Moerman, P Deprest, J Van Schoubroeck, D Timmerman, D Van Assche, F A Fryns, J P Producer: 20020131 In: American journal of medical genetics vol. 103 Availability: No items available. Save to lists Add to cart (remove)
	997.	Marden-Walker syndrome: case report, literature review and nosologic discussion. [electronic resource] by Schrander-Stumpel, C de Die-Smulders, C de Krom, M Schyns-Fleuran, S Hamel, B Jaeken, D Fryns, J P Producer: 19931014 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	998.	The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees. [electronic resource] by Claes, S Devriendt, K Lagae, L Ceulemans, B Dom, L Casaer, P Raeymaekers, P Cassiman, J J Fryns, J P Producer: 19971016 In: Annals of neurology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	999.	Semilobar holoprosencephaly in a 46,XY female fetus. [electronic resource] by Witters, I Moerman, P Muenke, M Van Assche, F A Devriendt, K Legius, E Van Schoubroeck, D Fryns, J P Producer: 20020131 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1000.	The acrofacial dysostoses--a wide spectrum of overlapping phenotypes. [electronic resource] by Dimitrov, B Balikova, I Bradinova, I Zahariev, D Popova, A Simeonov, E De Smet, L Devriendt, K Fryns, J P Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1120 results.