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R. Torra

Nephrology and Genetics Services

Hospital Clínic

Barcelona

Spain

[email]@medicina.ub.es

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Affiliations

Nephrology and Genetics Services, Hospital Clínic, Barcelona, Spain. 1998 - 1999
Servicio de Nefrología, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Universidad de Barcelona, Spain. 1999

References

Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease. Torra, R., Viribay, M., Tellería, D., Badenas, C., Watson, M., Harris, P., Darnell, A., San Millán, J.L. Kidney Int. (1999) [Pubmed]
A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2. Torra, R., Badenas, C., San Millán, J.L., Pérez-Oller, L., Estivill, X., Darnell, A. Am. J. Hum. Genet. (1999) [Pubmed]
Facilitated diagnosis of the contiguous gene syndrome: tuberous sclerosis and polycystic kidneys by means of haplotype studies. Torra, R., Badenas, C., Darnell, A., Camacho, J.A., Aspinwall, R., Harris, P.C., Estivill, X. Am. J. Kidney Dis. (1998) [Pubmed]