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P C Harris

Showing results (41-50 of 89) with videos related to

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Lancet (London, England)|December 14, 1991
Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite markerP C Harris, S Thomas, P J Ratcliffe, et al.
Human Mutation|August 3, 2000
Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease familiesM Koptides, R Mean, K Demetriou, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 19, 1998
Facilitated diagnosis of the contiguous gene syndrome: tuberous sclerosis and polycystic kidneys by means of haplotype studiesR Torra, C Badenas, A Darnell, et al.
Human Molecular Genetics|April 1, 1996
A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1)B Peral, A C Ong, J L San Millán, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 12, 1997
Neonatal presentation of autosomal dominant polycystic kidney disease with a maternal history of tuberous sclerosisM D Griffin, V Gamble, D S Milliner, et al.
American Journal of Human Genetics|April 1, 1993
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16)J Lamb, P C Harris, A O Wilkie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 19, 2004
Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysisM Sgro, S Rossetti, T Barozzino, et al.
Computers in Biology and Medicine|July 14, 2020
Semi-supervised labelling of the femur in a whole-body post-mortem CT database using deep learningC A Peña-Solórzano, D W Albrecht, R B Bassed, et al.
Circulation|August 1, 1989
Edema of cardiac origin. Studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureI S Anand, R Ferrari, G S Kalra, et al.
Human Molecular Genetics|April 1, 1995
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionB Peral, V Gamble, J L San Millán, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|December 14, 1991
Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite markerP C Harris, S Thomas, P J Ratcliffe, et al.
Human Mutation|August 3, 2000
Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease familiesM Koptides, R Mean, K Demetriou, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 19, 1998
Facilitated diagnosis of the contiguous gene syndrome: tuberous sclerosis and polycystic kidneys by means of haplotype studiesR Torra, C Badenas, A Darnell, et al.
Human Molecular Genetics|April 1, 1996
A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1)B Peral, A C Ong, J L San Millán, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 12, 1997
Neonatal presentation of autosomal dominant polycystic kidney disease with a maternal history of tuberous sclerosisM D Griffin, V Gamble, D S Milliner, et al.
American Journal of Human Genetics|April 1, 1993
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16)J Lamb, P C Harris, A O Wilkie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 19, 2004
Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysisM Sgro, S Rossetti, T Barozzino, et al.
Computers in Biology and Medicine|July 14, 2020
Semi-supervised labelling of the femur in a whole-body post-mortem CT database using deep learningC A Peña-Solórzano, D W Albrecht, R B Bassed, et al.
Circulation|August 1, 1989
Edema of cardiac origin. Studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureI S Anand, R Ferrari, G S Kalra, et al.
Human Molecular Genetics|April 1, 1995
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionB Peral, V Gamble, J L San Millán, et al.
Pageof 9