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J T Epplen

Showing results (181-190 of 365) with videos related to

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Human Genetics|April 1, 1987
Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variabilityJ T Epplen, J Chluba, C Hardt, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Morbus Huntington - a human genetic model diseaseJ T Epplen, M Gencik, A Epplen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1996
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutationL Schöls, G Amoiridis, J T Epplen, et al.
Fortschritte Der Neurologie-Psychiatrie|February 1, 1997
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]L Schöls, O Riess, G Amoiridis, et al.
Fetal Diagnosis and Therapy|July 27, 1999
Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 casesB Eiben, W Trawicki, W Hammans, et al.
EXS|January 1, 1993
Towards covering immunological genes with highly informative markers: a trans-species approachJ Buitkamp, W Schwaiger, C Epplen, et al.
Immunogenetics|January 1, 1985
A highly homologous T-cell receptor beta-chain variable region is expressed in mouse and human T cellsA Rinaldy, R B Wallace, M M Simon, et al.
Human Molecular Genetics|April 1, 1994
Dinucleotide repeat polymorphism in the IL2 and IL5RA genesC Epplen, G Frank, M Gomolka, et al.
Transfusion|October 1, 1992
Diagnosis of transfusion-associated graft-versus-host disease by genetic fingerprinting and polymerase chain reactionE Kunstmann, T Bocker, L Roewer, et al.
Neurology|July 25, 2007
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutationT Warnecke, T Duning, A Schwan, et al.
Pageof 37

Showing results (181-190 of 365) with videos related to

Sort By:
Pageof 37
Human Genetics|April 1, 1987
Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variabilityJ T Epplen, J Chluba, C Hardt, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Morbus Huntington - a human genetic model diseaseJ T Epplen, M Gencik, A Epplen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1996
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutationL Schöls, G Amoiridis, J T Epplen, et al.
Fortschritte Der Neurologie-Psychiatrie|February 1, 1997
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]L Schöls, O Riess, G Amoiridis, et al.
Fetal Diagnosis and Therapy|July 27, 1999
Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 casesB Eiben, W Trawicki, W Hammans, et al.
EXS|January 1, 1993
Towards covering immunological genes with highly informative markers: a trans-species approachJ Buitkamp, W Schwaiger, C Epplen, et al.
Immunogenetics|January 1, 1985
A highly homologous T-cell receptor beta-chain variable region is expressed in mouse and human T cellsA Rinaldy, R B Wallace, M M Simon, et al.
Human Molecular Genetics|April 1, 1994
Dinucleotide repeat polymorphism in the IL2 and IL5RA genesC Epplen, G Frank, M Gomolka, et al.
Transfusion|October 1, 1992
Diagnosis of transfusion-associated graft-versus-host disease by genetic fingerprinting and polymerase chain reactionE Kunstmann, T Bocker, L Roewer, et al.
Neurology|July 25, 2007
A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutationT Warnecke, T Duning, A Schwan, et al.
Pageof 37