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M SINISCALCO

Showing results (31-40 of 51) with videos related to

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Human Genetics|January 1, 1984
Old and new genetics help ordering loci at the telomere of the human X-chromosome long armM Purrello, R Nussbaum, A Rinaldi, et al.
American Journal of Medical Genetics|August 9, 1996
Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probeM Grasso, L Perroni, F Dagna-Bricarelli, et al.
Genomics|September 1, 1992
Chromosomal assignment of human YAC clones by fluorescence in situ hybridization: use of single-yeast-colony PCR and multiple labelingA Baldini, M Ross, D Nizetic, et al.
Human Genetics|September 1, 1986
The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PDC Webster, G Filippi, A Rinaldi, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA cluster (RNU1) within 400 kb of the chromosome region 1p36.1M Romani, A Baldini, E V Volpi, et al.
American Journal of Human Genetics|April 1, 1990
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectM Rocchi, N Archidiacono, A Rinaldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Chromosomes of older humans are more prone to aminopterine-induced breakageD Esposito, G Fassina, P Szabo, et al.
American Journal of Medical Genetics|November 6, 1995
X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studiesR Robledo, P Melis, E Schillinger, et al.
The EMBO Journal|March 1, 1985
The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3M Purrello, B Alhadeff, D Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Genetics|January 1, 1984
Old and new genetics help ordering loci at the telomere of the human X-chromosome long armM Purrello, R Nussbaum, A Rinaldi, et al.
American Journal of Medical Genetics|August 9, 1996
Premutation for the Martin-Bell syndrome analyzed in a large Sardinian family: III. Molecular analysis with the StB12.3 probeM Grasso, L Perroni, F Dagna-Bricarelli, et al.
Genomics|September 1, 1992
Chromosomal assignment of human YAC clones by fluorescence in situ hybridization: use of single-yeast-colony PCR and multiple labelingA Baldini, M Ross, D Nizetic, et al.
Human Genetics|September 1, 1986
The myoblast defect identified in Duchenne muscular dystrophy is not a primary expression of the DMD mutation. Clonal analysis of myoblasts from five double heterozygotes for two X-linked loci: DMD and G6PDC Webster, G Filippi, A Rinaldi, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA cluster (RNU1) within 400 kb of the chromosome region 1p36.1M Romani, A Baldini, E V Volpi, et al.
American Journal of Human Genetics|April 1, 1990
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectM Rocchi, N Archidiacono, A Rinaldi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Chromosomes of older humans are more prone to aminopterine-induced breakageD Esposito, G Fassina, P Szabo, et al.
American Journal of Medical Genetics|November 6, 1995
X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studiesR Robledo, P Melis, E Schillinger, et al.
The EMBO Journal|March 1, 1985
The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3M Purrello, B Alhadeff, D Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972
Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.
Pageof 6