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	1.	CFC syndrome: report of familial cases. [electronic resource] by Lecora, M Parenti, G Andria, G Producer: 19970509 In: Clinical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Polysyndactyly and trigonocephaly with partial agenesis of corpus callosum. [electronic resource] by Guzzetta, V Lecora, M Rossi, G Berni Canani, M Andria, G Producer: 19960927 In: Clinical dysmorphology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New case of bilateral upper limb amelia, facial clefts, and renal hypoplasia. [electronic resource] by Pierri, N B Lecora, M Passariello, A Scala, I Andria, G Producer: 20000421 In: American journal of medical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Immunological disorder and Hirschsprung disease in round femoral inferior epiphysis dysplasia. [electronic resource] by Lecora, M Parenti, G Iaccarino, E Scarano, G Cucchiara, S Andria, G Producer: 19950816 In: Clinical dysmorphology vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	5.	T cell activation deficiency associated with an aberrant pattern of protein tyrosine phosphorylation after CD3 perturbation in Down's syndrome. [electronic resource] by Scotese, I Gaetaniello, L Matarese, G Lecora, M Racioppi, L Pignata, C Producer: 19981027 In: Pediatric research vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Geleophysic dysplasia: 7-year follow-up study of a patient with an intermediate form. [electronic resource] by Titomanlio, L Della Casa, R Lecora, M Farina, V Sebastio, G Andria, G Parenti, G Producer: 19990910 In: American journal of medical genetics vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	7.	Growth retardation, developmental delay, distinctive face, multiple endocrine abnormalities, and adenylyl cyclase dysfunction: a new syndrome? [electronic resource] by Salerno, M Amabile, G Mandato, C Di Maio, S Lecora, M Avvedimento, E V Andria, G Producer: 20040218 In: American journal of medical genetics. Part A vol. 120A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Prenatal ultrasound diagnosis of Roberts syndrome in a family with negative history. [electronic resource] by Paladini, D Palmieri, S Lecora, M Perone, L Di Meglio, A D'Armiento, M Cascioli, C Martinelli, P Producer: 19960910 In: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Clinical and biochemical screening for Smith-Lemli-Opitz syndrome. Italian SLOS Collaborative Group. [electronic resource] by Guzzetta, V De Fabiani, E Galli, G Colombo, C Corso, G Lecora, M Parenti, G Strisciuglio, P Andria, G Producer: 19961210 In: Acta paediatrica (Oslo, Norway : 1992) vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Phenylketonuria in Italy: distinct distribution pattern of three mutations of the phenylalanine hydroxylase gene. [electronic resource] by Guzzetta, V Bonapace, G Dianzani, I Parenti, G Lecora, M Giannattasio, S Concolino, D Strisciuglio, P Sebastio, G Andria, G Producer: 19971106 In: Journal of inherited metabolic disease vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients. [electronic resource] by Grasso, M Faravelli, F Lo Nigro, C Chiurazzi, P Sperandeo, M P Argusti, A Pomponi, M G Lecora, M Sebastio, G F Perroni, L Andria, G Neri, G Bricarelli, F D Producer: 20000517 In: American journal of medical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter study. [electronic resource] by Bonamico, M Mariani, P Danesi, H M Crisogianni, M Failla, P Gemme, G Quartino, A R Giannotti, A Castro, M Balli, F Lecora, M Andria, G Guariso, G Gabrielli, O Catassi, C Lazzari, R Balocco, N A De Virgiliis, S Culasso, F Romano, C Producer: 20011025 In: Journal of pediatric gastroenterology and nutrition vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)