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	21.	Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families. [electronic resource] by Torra, R Badenas, C Peral, B Darnell, A Serra, E Gamble, V Turco, A E Harris, P C Estivill, X Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresia. [electronic resource] by Turco, A E Peissel, B Rossetti, S Selicorni, A Manoukian, S Brusasco, A Tadini, G Galimberti, A Tassis, B Turolla, L Producer: 19940224 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformations. [electronic resource] by Turco, A E Padovani, E M Chiaffoni, G P Peissel, B Rossetti, S Marcolongo, A Gammaro, L Maschio, G Pignatti, P F Producer: 19930805 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney disease. [electronic resource] by Turco, A E Rossetti, S Bresin, E Corrà, S Restagno, G Carbonara, A De Prisco, O Gammaro, L Maschio, G Pignatti, P F Producer: 19970513 In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association vol. 11 Suppl 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome. [electronic resource] by Turco, A E Rossetti, S Biasi, M O Rizzoni, G Massella, L Saarinen, N H Renieri, A Pignatti, P F De Marchi, M Producer: 19961205 In: Clinical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects. [electronic resource] by Nomura, H Turco, A E Pei, Y Kalaydjieva, L Schiavello, T Weremowicz, S Ji, W Morton, C C Meisler, M Reeders, S T Zhou, J Producer: 19981112 In: The Journal of biological chemistry vol. 273 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an update. [electronic resource] by Turco, A E Bresin, E Rossetti, S Englisch, S Pignatti, P F Gammaro, L Maschio, G Bendetti, M Li Vecchi, M Ferrantelli, A Cerasola, G Stiasny, B Schulze, B Producer: 19980127 In: Contributions to nephrology vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers. [electronic resource] by Barker, D F Fain, P R Goldgar, D E Dietz-Band, J N Turco, A E Kashtan, C E Gregory, M C Tryggvason, K Skolnick, M H Atkin, C L Producer: 19920204 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Missense mutations in the COL4A5 gene in patients with X-linked Alport syndrome. [electronic resource] by Neri, T M Zanelli, P De Palma, G Savi, M Rossetti, S Turco, A E Pignatti, G F Galli, L Bruttini, M Renieri, A Mingarelli, R Trivelli, A Pinciaroli, A R Ragaiolo, M Rizzoni, G F De Marchi, M Producer: 19990630 In: Human mutation vol. Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)