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L Mandel

Showing results (161-170 of 451) with videos related to

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Human Genetics|January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locusG Camerino, I Oberlé, D Drayna, et al.
Human Genetics|April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosomeA Vincent, C Kretz, I Oberlé, et al.
Biochimica Et Biophysica Acta|June 20, 1990
Avian kidney mitochondrial hemeprotein P-4501 alpha: isolation, characterization and NADPH-ferredoxin reductase-dependent activityM L Mandel, S J Swartz, J G Ghazarian
Radiobiologia, Radiotherapia|January 1, 1980
[Results of combined therapy of malignant renal tumours (author's transl)]S Mau, K H Riessbeck, L Mandel, et al.
Nature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research|May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armM Koenig, G Camerino, R Heilig, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Nucleic Acids Research|July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y geneR Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research|July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.
Pageof 46

Showing results (161-170 of 451) with videos related to

Sort By:
Pageof 46
Human Genetics|January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locusG Camerino, I Oberlé, D Drayna, et al.
Human Genetics|April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosomeA Vincent, C Kretz, I Oberlé, et al.
Biochimica Et Biophysica Acta|June 20, 1990
Avian kidney mitochondrial hemeprotein P-4501 alpha: isolation, characterization and NADPH-ferredoxin reductase-dependent activityM L Mandel, S J Swartz, J G Ghazarian
Radiobiologia, Radiotherapia|January 1, 1980
[Results of combined therapy of malignant renal tumours (author's transl)]S Mau, K H Riessbeck, L Mandel, et al.
Nature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research|May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armM Koenig, G Camerino, R Heilig, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Nucleic Acids Research|July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y geneR Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research|July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.
Pageof 46