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D Ravine

Showing results (1-10 of 41) with videos related to

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Journal of Inherited Metabolic Disease|July 17, 1999
Automated mutation analysisD Ravine
QJM : Monthly Journal of the Association of Physicians|February 1, 1997
Adult-onset genetic disease: mechanisms, analysis and predictionD Ravine, D N Cooper
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, M MacDonald, D Ravine
Journal of Medical Genetics|October 1, 1980
Genetic inheritance of susceptibility to tinea imbricataD Ravine, K J Turner, M P Alpers
European Journal of Pediatrics|April 1, 1993
Non-specific elevation of immunoreactive trypsinogen in sick infantsD Ravine, R I Francis, D M Danks
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1993
An ultrasound renal cyst prevalence survey: specificity data for inherited renal cystic diseasesD Ravine, R N Gibson, J Donlan, et al.
The Medical Journal of Australia|May 20, 1991
Perceptions of genetic risk in individuals with a one in two chance of developing autosomal dominant polycystic kidney diseaseD Ravine, L R McGregor, R G Walker, et al.
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2000
Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindredN Hateboer, M Buchalter, S J Davies, et al.
Human Genetics|April 1, 1998
Novel and recurrent mutations in the PKD1 (polycystic kidney disease) geneC Daniells, M Maheshwar, L Lazarou, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Journal of Inherited Metabolic Disease|July 17, 1999
Automated mutation analysisD Ravine
QJM : Monthly Journal of the Association of Physicians|February 1, 1997
Adult-onset genetic disease: mechanisms, analysis and predictionD Ravine, D N Cooper
Prenatal Diagnosis|October 16, 1999
Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, M MacDonald, D Ravine
Journal of Medical Genetics|October 1, 1980
Genetic inheritance of susceptibility to tinea imbricataD Ravine, K J Turner, M P Alpers
European Journal of Pediatrics|April 1, 1993
Non-specific elevation of immunoreactive trypsinogen in sick infantsD Ravine, R I Francis, D M Danks
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1993
An ultrasound renal cyst prevalence survey: specificity data for inherited renal cystic diseasesD Ravine, R N Gibson, J Donlan, et al.
The Medical Journal of Australia|May 20, 1991
Perceptions of genetic risk in individuals with a one in two chance of developing autosomal dominant polycystic kidney diseaseD Ravine, L R McGregor, R G Walker, et al.
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 31, 2000
Co-occurrence of autosomal dominant polycystic kidney disease and Marfan syndrome in a kindredN Hateboer, M Buchalter, S J Davies, et al.
Human Genetics|April 1, 1998
Novel and recurrent mutations in the PKD1 (polycystic kidney disease) geneC Daniells, M Maheshwar, L Lazarou, et al.
Pageof 5