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A E Turco

Showing results (21-30 of 29) with videos related to

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Journal of Perinatal Medicine|January 1, 1995
Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case reportA E Turco, E M Padovani, B Peissel, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresiaA E Turco, B Peissel, S Rossetti, et al.
Journal of Medical Genetics|May 1, 1993
Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformationsA E Turco, E M Padovani, G P Chiaffoni, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Clinical Genetics|November 1, 1995
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndromeA E Turco, S Rossetti, M O Biasi, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
Contributions to Nephrology|January 1, 1997
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an updateA E Turco, E Bresin, S Rossetti, et al.
Human Genetics|December 1, 1991
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markersD F Barker, P R Fain, D E Goldgar, et al.
Human Mutation|February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndromeT M Neri, P Zanelli, G De Palma, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Perinatal Medicine|January 1, 1995
Gene linkage analysis and DNA based detection of autosomal dominant polycystic kidney disease (ADPKD) in a newborn infant. Case reportA E Turco, E M Padovani, B Peissel, et al.
American Journal of Medical Genetics|December 1, 1993
Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disease and autosomal recessive junctional epidermolysis bullosa with pyloric atresiaA E Turco, B Peissel, S Rossetti, et al.
Journal of Medical Genetics|May 1, 1993
Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformationsA E Turco, E M Padovani, G P Chiaffoni, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Clinical Genetics|November 1, 1995
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndromeA E Turco, S Rossetti, M O Biasi, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
Contributions to Nephrology|January 1, 1997
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an updateA E Turco, E Bresin, S Rossetti, et al.
Human Genetics|December 1, 1991
High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markersD F Barker, P R Fain, D E Goldgar, et al.
Human Mutation|February 6, 1998
Missense mutations in the COL4A5 gene in patients with X-linked Alport syndromeT M Neri, P Zanelli, G De Palma, et al.
Pageof 3