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R HEILIG

Showing results (31-40 of 67) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 1999
Genetic linkage of Meleda disease to chromosome 8qterJ Fischer, B Bouadjar, R Heilig, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Isolated dystrophin molecules as seen by electron microscopyF Pons, N Augier, R Heilig, et al.
American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 19, 2012
Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patientsM Fiore, N Firah, X Pillois, et al.
Nature|July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosomeR Heilig, C Lemaire, J L Mandel, et al.
Nucleic Acids Research|June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actinA Hanauer, M Levin, R Heilig, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences|May 1, 1991
Slit scan flow cytometry of isolated chromosomes following fluorescence hybridization: an approach of online screening for specific chromosomes and chromosome translocationsM Hausmann, G Dudin, J A Aten, et al.
American Journal of Human Genetics|April 1, 1990
Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosomeR Feil, G Palmieri, M d'Urso, et al.
The EMBO Journal|August 1, 1984
Actin-like sequences are present on human X and Y chromosomesR Heilig, A Hanauer, K H Grzeschik, et al.
American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|January 15, 1999
Genetic linkage of Meleda disease to chromosome 8qterJ Fischer, B Bouadjar, R Heilig, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Isolated dystrophin molecules as seen by electron microscopyF Pons, N Augier, R Heilig, et al.
American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 19, 2012
Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patientsM Fiore, N Firah, X Pillois, et al.
Nature|July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosomeR Heilig, C Lemaire, J L Mandel, et al.
Nucleic Acids Research|June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actinA Hanauer, M Levin, R Heilig, et al.
Zeitschrift Fur Naturforschung. C, Journal of Biosciences|May 1, 1991
Slit scan flow cytometry of isolated chromosomes following fluorescence hybridization: an approach of online screening for specific chromosomes and chromosome translocationsM Hausmann, G Dudin, J A Aten, et al.
American Journal of Human Genetics|April 1, 1990
Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosomeR Feil, G Palmieri, M d'Urso, et al.
The EMBO Journal|August 1, 1984
Actin-like sequences are present on human X and Y chromosomesR Heilig, A Hanauer, K H Grzeschik, et al.
American Journal of Human Genetics|March 11, 2000
Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisisS Saunier, J Calado, F Benessy, et al.
Pageof 7