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S Rudnik-Schöneborn

Showing results (1-10 of 82) with videos related to

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Fortschritte Der Neurologie-Psychiatrie|January 21, 2015
[Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy]Josef Finsterer, S Rudnik-Schöneborn
Kidney & Blood Pressure Research|January 1, 1996
Current status of DNA diagnosis for hereditary nephropathiesK Zerres, S Rudnik-Schöneborn
Archives of Neurology|May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classificationsK Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics|June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?S Rudnik-Schöneborn, K Zerres
Clinical Genetics|May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibshipsF Deget, S Rudnik-Schöneborn, K Zerres
Clinical Nephrology|October 13, 2001
DNA diagnosis in hereditary nephropathiesK Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD|May 1, 1997
Spinal muscular atrophy--clinical and genetic correlationsK Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics|June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4K Zerres, G Mücher, S Rudnik-Schöneborn
American Journal of Human Genetics|July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophyS Rudnik-Schöneborn, B Wirth, K Zerres
Journal of Medical Genetics|July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische NephrologieK Zerres, S Rudnik-Schöneborn, F Deget
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Fortschritte Der Neurologie-Psychiatrie|January 21, 2015
[Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy]Josef Finsterer, S Rudnik-Schöneborn
Kidney & Blood Pressure Research|January 1, 1996
Current status of DNA diagnosis for hereditary nephropathiesK Zerres, S Rudnik-Schöneborn
Archives of Neurology|May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classificationsK Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics|June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?S Rudnik-Schöneborn, K Zerres
Clinical Genetics|May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibshipsF Deget, S Rudnik-Schöneborn, K Zerres
Clinical Nephrology|October 13, 2001
DNA diagnosis in hereditary nephropathiesK Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD|May 1, 1997
Spinal muscular atrophy--clinical and genetic correlationsK Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics|June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4K Zerres, G Mücher, S Rudnik-Schöneborn
American Journal of Human Genetics|July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophyS Rudnik-Schöneborn, B Wirth, K Zerres
Journal of Medical Genetics|July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische NephrologieK Zerres, S Rudnik-Schöneborn, F Deget
Pageof 9