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O Riess

Showing results (51-60 of 144) with videos related to

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Human Molecular Genetics|September 1, 1993
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish familiesA Nørremølle, O Riess, J T Epplen, et al.
Human Molecular Genetics|June 1, 1995
Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patientsL Schöls, A M Vieira-Saecker, S Schöls, et al.
Journal of Medical Genetics|February 24, 2001
Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)D Wieczorek, M Krause, F Majewski, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Human Genetics|October 13, 2000
Genetic background of apparently idiopathic sporadic cerebellar ataxiaL Schöls, S Szymanski, S Peters, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletionD Wieczorek, M Krause, F Majewski, et al.
The Biochemical Journal|November 10, 1998
Isolation and characterization of the rat huntingtin promoterC Holzmann, W Mäueler, D Petersohn, et al.
Onkologie|December 14, 2004
Multiple organ failure due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variantA Lazar, U A Mau-Holzmann, H Kolb, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Analysis of mitochondrial targeting sequence and coding region polymorphisms of the manganese superoxide dismutase gene in German Parkinson disease patientsE M Grasbon-Frodl, S Kösel, O Riess, et al.
Human Molecular Genetics|September 1, 1993
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German originC Zühlke, O Riess, K Schröder, et al.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|September 1, 1993
Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish familiesA Nørremølle, O Riess, J T Epplen, et al.
Human Molecular Genetics|June 1, 1995
Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patientsL Schöls, A M Vieira-Saecker, S Schöls, et al.
Journal of Medical Genetics|February 24, 2001
Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)D Wieczorek, M Krause, F Majewski, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Human Genetics|October 13, 2000
Genetic background of apparently idiopathic sporadic cerebellar ataxiaL Schöls, S Szymanski, S Peters, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletionD Wieczorek, M Krause, F Majewski, et al.
The Biochemical Journal|November 10, 1998
Isolation and characterization of the rat huntingtin promoterC Holzmann, W Mäueler, D Petersohn, et al.
Onkologie|December 14, 2004
Multiple organ failure due to 5-fluorouracil chemotherapy in a patient with a rare dihydropyrimidine dehydrogenase gene variantA Lazar, U A Mau-Holzmann, H Kolb, et al.
Biochemical and Biophysical Research Communications|March 2, 1999
Analysis of mitochondrial targeting sequence and coding region polymorphisms of the manganese superoxide dismutase gene in German Parkinson disease patientsE M Grasbon-Frodl, S Kösel, O Riess, et al.
Human Molecular Genetics|September 1, 1993
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German originC Zühlke, O Riess, K Schröder, et al.
Pageof 15