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P Nürnberg

Showing results (11-20 of 115) with videos related to

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Human Heredity|May 9, 2000
Mapping genes for polygenic disorders: considerations for study design in the complex trait of inflammatory bowel diseaseJ Hampe, T Wienker, P Nürnberg, et al.
Biomedica Biochimica Acta|January 1, 1983
One-step purification of L-type pyruvate kinase by microimmunoaffinity chromatographyP Nürnberg, G Jacobasch, F Noll, et al.
Electrophoresis|March 21, 1998
A novel standardization method for two-dimensional DNA fingerprintsJ Hampe, R Mrowka, K Marczinek, et al.
Human Genetics|March 1, 1993
Changes of telomere lengths in human intracranial tumoursP Nürnberg, G Thiel, F Weber, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1997
Complete genomic sequence of the human PK-L/R-gene includes four intragenic polymorphisms defining different haplotype backgrounds of normal and mutant PK-genesC Lenzner, P Nürnberg, G Jacobasch, et al.
Clinical Endocrinology|January 1, 1996
A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidusF Rauch, C Lenzner, P Nürnberg, et al.
Human Molecular Genetics|March 1, 1994
Trinucleotide repeat polymorphism at the PKLR locusC Lenzner, G Jacobasch, A Reis, et al.
Electrophoresis|August 6, 1999
Changes in methylation patterns identified by two-dimensional DNA fingerprintingK Uhlmann, K Marczinek, J Hampe, et al.
Electrophoresis|September 1, 1995
Increased microsatellite variability in Macaca mulatta compared to humans due to a large scale deletion/insertion event during primate evolutionM Kayser, P Nürnberg, F Bercovitch, et al.
American Journal of Medical Genetics|April 6, 1999
McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patientS Tinschert, H Gerl, A Gewies, et al.
Pageof 12

Showing results (11-20 of 115) with videos related to

Sort By:
Pageof 12
Human Heredity|May 9, 2000
Mapping genes for polygenic disorders: considerations for study design in the complex trait of inflammatory bowel diseaseJ Hampe, T Wienker, P Nürnberg, et al.
Biomedica Biochimica Acta|January 1, 1983
One-step purification of L-type pyruvate kinase by microimmunoaffinity chromatographyP Nürnberg, G Jacobasch, F Noll, et al.
Electrophoresis|March 21, 1998
A novel standardization method for two-dimensional DNA fingerprintsJ Hampe, R Mrowka, K Marczinek, et al.
Human Genetics|March 1, 1993
Changes of telomere lengths in human intracranial tumoursP Nürnberg, G Thiel, F Weber, et al.
DNA Sequence : the Journal of DNA Sequencing and Mapping|January 1, 1997
Complete genomic sequence of the human PK-L/R-gene includes four intragenic polymorphisms defining different haplotype backgrounds of normal and mutant PK-genesC Lenzner, P Nürnberg, G Jacobasch, et al.
Clinical Endocrinology|January 1, 1996
A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidusF Rauch, C Lenzner, P Nürnberg, et al.
Human Molecular Genetics|March 1, 1994
Trinucleotide repeat polymorphism at the PKLR locusC Lenzner, G Jacobasch, A Reis, et al.
Electrophoresis|August 6, 1999
Changes in methylation patterns identified by two-dimensional DNA fingerprintingK Uhlmann, K Marczinek, J Hampe, et al.
Electrophoresis|September 1, 1995
Increased microsatellite variability in Macaca mulatta compared to humans due to a large scale deletion/insertion event during primate evolutionM Kayser, P Nürnberg, F Bercovitch, et al.
American Journal of Medical Genetics|April 6, 1999
McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patientS Tinschert, H Gerl, A Gewies, et al.
Pageof 12