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D Toniolo

Showing results (61-70 of 93) with videos related to

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Nucleic Acids Research|March 25, 1986
Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding regionM G Persico, G Viglietto, G Martini, et al.
American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
Genomics|May 1, 1994
The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280M C Patrosso, M Repetto, A Villa, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Journal of Medical Genetics|July 17, 2008
Epigenetic analysis of the critical region I for premature ovarian failure: demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosomeF Rizzolio, T Pramparo, C Sala, et al.
Nucleic Acids Research|May 25, 1991
Molecular cloning and analysis of the fragile X region in manA Dietrich, P Kioschis, A P Monaco, et al.
Genomics|February 15, 1997
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21C Sala, G Arrigo, G Torri, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptorE Maestrini, L Tamagnone, P Longati, et al.
Immunodeficiency|January 1, 1993
Molecular analysis of X-linked immunodeficiency with hyper-IgM and X-linked lymphoproliferative syndromeL D Notarangelo, E Mantuano, S Bione, et al.
Science (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.
Pageof 10

Showing results (61-70 of 93) with videos related to

Sort By:
Pageof 10
Nucleic Acids Research|March 25, 1986
Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding regionM G Persico, G Viglietto, G Martini, et al.
American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
Genomics|May 1, 1994
The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280M C Patrosso, M Repetto, A Villa, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Journal of Medical Genetics|July 17, 2008
Epigenetic analysis of the critical region I for premature ovarian failure: demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosomeF Rizzolio, T Pramparo, C Sala, et al.
Nucleic Acids Research|May 25, 1991
Molecular cloning and analysis of the fragile X region in manA Dietrich, P Kioschis, A P Monaco, et al.
Genomics|February 15, 1997
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21C Sala, G Arrigo, G Torri, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
A family of transmembrane proteins with homology to the MET-hepatocyte growth factor receptorE Maestrini, L Tamagnone, P Longati, et al.
Immunodeficiency|January 1, 1993
Molecular analysis of X-linked immunodeficiency with hyper-IgM and X-linked lymphoproliferative syndromeL D Notarangelo, E Mantuano, S Bione, et al.
Science (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.
Pageof 10