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Showing results (81-90 of 115) with videos related to

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Human Genetics|January 1, 1990
Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panelA Jobs, D Klein-Bölting, A S Jandel, et al.
Lancet (London, England)|June 20, 1992
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung diseaseW Poller, J P Faber, S Scholz, et al.
The EMBO Journal|August 1, 1990
Regeneration-associated high level expression of apolipoprotein D mRNA in endoneurial fibroblasts of peripheral nerveP Spreyer, H Schaal, G Kuhn, et al.
Genomics|November 1, 1994
A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNAG Mertes, M Ludwig, B Finkelnburg, et al.
American Journal of Human Genetics|March 1, 1987
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7S Zengerling, L C Tsui, K H Grzeschik, et al.
Blood|October 7, 2000
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicismJ Oldenburg, S Rost, O El-Maarri, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|March 1, 1989
Prenatal diagnosis of cystic fibrosisW Kampmann, L Mathy, K H Grzeschik, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2001
Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutationsA A Timur, A Gürgey, G Aktuglu, et al.
Human Genetics|April 1, 1988
Phenylketonuria: distribution of DNA diagnostic patterns in German familiesC Aulehla-Scholz, M Vorgerd, E Sautter, et al.
Human Genetics|September 1, 1990
The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic originC Aulehla-Scholz, R Kaiser, J Weber, et al.
Pageof 12

Showing results (81-90 of 115) with videos related to

Sort By:
Pageof 12
Human Genetics|January 1, 1990
Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panelA Jobs, D Klein-Bölting, A S Jandel, et al.
Lancet (London, England)|June 20, 1992
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung diseaseW Poller, J P Faber, S Scholz, et al.
The EMBO Journal|August 1, 1990
Regeneration-associated high level expression of apolipoprotein D mRNA in endoneurial fibroblasts of peripheral nerveP Spreyer, H Schaal, G Kuhn, et al.
Genomics|November 1, 1994
A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNAG Mertes, M Ludwig, B Finkelnburg, et al.
American Journal of Human Genetics|March 1, 1987
Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7S Zengerling, L C Tsui, K H Grzeschik, et al.
Blood|October 7, 2000
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicismJ Oldenburg, S Rost, O El-Maarri, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|March 1, 1989
Prenatal diagnosis of cystic fibrosisW Kampmann, L Mathy, K H Grzeschik, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 14, 2001
Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutationsA A Timur, A Gürgey, G Aktuglu, et al.
Human Genetics|April 1, 1988
Phenylketonuria: distribution of DNA diagnostic patterns in German familiesC Aulehla-Scholz, M Vorgerd, E Sautter, et al.
Human Genetics|September 1, 1990
The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic originC Aulehla-Scholz, R Kaiser, J Weber, et al.
Pageof 12