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K Olek

Showing results (71-80 of 115) with videos related to

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Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1988
Evaluation of random cDNA clones as probes for human restriction fragment length polymorphismsC Wappenschmidt, M Higuchi, C Meisen, et al.
American Journal of Human Genetics|December 1, 1993
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia AJ Oldenburg, R Schwaab, T Grimm, et al.
American Journal of Human Genetics|December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M alleleJ P Faber, W Poller, S Weidinger, et al.
Blood|August 15, 1989
Molecular defects in hemophilia A: identification and characterization of mutations in the factor VIII gene and family analysisM Higuchi, L Kochhan, R Schwaab, et al.
American Journal of Human Genetics|October 1, 1990
Identical point mutations in the factor VIII gene that have different clinical manifestations of hemophilia AR Schwaab, M Ludwig, J Oldenburg, et al.
Journal of Hepatology|July 1, 1993
The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung diseaseJ P Faber, W Poller, K Olek, et al.
Nucleic Acids Research|August 11, 1987
A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5)H D Orzechowski, J Hennig, P Winter, et al.
Science (New York, N.Y.)|July 17, 1992
Recovery from hemophilia B Leyden: an androgen-responsive element in the factor IX promoterM Crossley, M Ludwig, K M Stowell, et al.
Human Genetics|December 1, 1988
Cystic fibrosis: typing 89 German families with linked DNA probesJ Weber, C Aulehla-Scholz, R Kaiser, et al.
American Journal of Human Genetics|July 1, 1989
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia BM Ludwig, R Schwaab, A Eigel, et al.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1988
Evaluation of random cDNA clones as probes for human restriction fragment length polymorphismsC Wappenschmidt, M Higuchi, C Meisen, et al.
American Journal of Human Genetics|December 1, 1993
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia AJ Oldenburg, R Schwaab, T Grimm, et al.
American Journal of Human Genetics|December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M alleleJ P Faber, W Poller, S Weidinger, et al.
Blood|August 15, 1989
Molecular defects in hemophilia A: identification and characterization of mutations in the factor VIII gene and family analysisM Higuchi, L Kochhan, R Schwaab, et al.
American Journal of Human Genetics|October 1, 1990
Identical point mutations in the factor VIII gene that have different clinical manifestations of hemophilia AR Schwaab, M Ludwig, J Oldenburg, et al.
Journal of Hepatology|July 1, 1993
The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung diseaseJ P Faber, W Poller, K Olek, et al.
Nucleic Acids Research|August 11, 1987
A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5)H D Orzechowski, J Hennig, P Winter, et al.
Science (New York, N.Y.)|July 17, 1992
Recovery from hemophilia B Leyden: an androgen-responsive element in the factor IX promoterM Crossley, M Ludwig, K M Stowell, et al.
Human Genetics|December 1, 1988
Cystic fibrosis: typing 89 German families with linked DNA probesJ Weber, C Aulehla-Scholz, R Kaiser, et al.
American Journal of Human Genetics|July 1, 1989
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia BM Ludwig, R Schwaab, A Eigel, et al.
Pageof 12