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P Nürnberg

Showing results (21-30 of 115) with videos related to

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Blood|March 1, 1997
Molecular analysis of 29 pyruvate kinase-deficient patients from central Europe with hereditary hemolytic anemiaC Lenzner, P Nürnberg, G Jacobasch, et al.
Electrophoresis|August 7, 1998
Bipolar clamping improves the sensitivity of mutation detection by temperature gradient gel electrophoresisC Gille, A Gille, P Booms, et al.
The British Journal of Surgery|April 14, 1999
Experience with the Mainz modification of ureterosigmoidostomyJ H Jongen, N P Nürnberg, M Stöckle, et al.
Nucleic Acids Research|April 12, 2011
Complete characterization of the edited transcriptome of the mitochondrion of Physarum polycephalum using deep sequencing of RNAR Bundschuh, J Altmüller, C Becker, et al.
Human Mutation|January 1, 1996
Recurrent 2-bp deletion in exon 10c of the NF1 gene in two cases of von Recklinghausen neurofibromatosisP N Robinson, A Buske, R Neumann, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001
Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaquesA Widdig, P Nürnberg, M Krawczak, et al.
Human Molecular Genetics|August 1, 1995
On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1S Hoffmeyer, G Assum, J Griesser, et al.
Biochemical and Biophysical Research Communications|September 25, 1995
Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 geneA Böddrich, J Griesser, D Horn, et al.
Archives of Neurology|April 1, 1997
'Complicated' autosomal dominant familial spastic paraplegia is genetically distinct from 'pure' formsH Meierkord, P Nürnberg, A Mainz, et al.
Human Antibodies and Hybridomas|October 1, 1992
Oligonucleotide fingerprinting as a means to identify and survey long-term cultured B cell hybridomas and T cell linesJ Hampe, P Nürnberg, C Epplen, et al.
Pageof 12

Showing results (21-30 of 115) with videos related to

Sort By:
Pageof 12
Blood|March 1, 1997
Molecular analysis of 29 pyruvate kinase-deficient patients from central Europe with hereditary hemolytic anemiaC Lenzner, P Nürnberg, G Jacobasch, et al.
Electrophoresis|August 7, 1998
Bipolar clamping improves the sensitivity of mutation detection by temperature gradient gel electrophoresisC Gille, A Gille, P Booms, et al.
The British Journal of Surgery|April 14, 1999
Experience with the Mainz modification of ureterosigmoidostomyJ H Jongen, N P Nürnberg, M Stöckle, et al.
Nucleic Acids Research|April 12, 2011
Complete characterization of the edited transcriptome of the mitochondrion of Physarum polycephalum using deep sequencing of RNAR Bundschuh, J Altmüller, C Becker, et al.
Human Mutation|January 1, 1996
Recurrent 2-bp deletion in exon 10c of the NF1 gene in two cases of von Recklinghausen neurofibromatosisP N Robinson, A Buske, R Neumann, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2001
Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaquesA Widdig, P Nürnberg, M Krawczak, et al.
Human Molecular Genetics|August 1, 1995
On unequal allelic expression of the neurofibromin gene in neurofibromatosis type 1S Hoffmeyer, G Assum, J Griesser, et al.
Biochemical and Biophysical Research Communications|September 25, 1995
Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 geneA Böddrich, J Griesser, D Horn, et al.
Archives of Neurology|April 1, 1997
'Complicated' autosomal dominant familial spastic paraplegia is genetically distinct from 'pure' formsH Meierkord, P Nürnberg, A Mainz, et al.
Human Antibodies and Hybridomas|October 1, 1992
Oligonucleotide fingerprinting as a means to identify and survey long-term cultured B cell hybridomas and T cell linesJ Hampe, P Nürnberg, C Epplen, et al.
Pageof 12