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M Rocchi

Showing results (91-100 of 309) with videos related to

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Genomics|January 20, 1995
Comparative mapping of human alphoid sequences in great apes using fluorescence in situ hybridizationN Archidiacono, R Antonacci, R Marzella, et al.
Advances in Neurology|January 1, 1988
X-linked muscular dystrophies: studies through functional assay and DNA polymorphismsG Romeo, M Rocchi, L Roncuzzi, et al.
Prenatal Diagnosis|May 1, 1985
Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytesM Rocchi, V Pecile, N Archidiacono, et al.
Cytogenetics and Cell Genetics|July 28, 2001
Genomic organization and mapping of the gene (SLC25A19) encoding the human mitochondrial deoxynucleotide carrier (DNC)V Iacobazzi, M Ventura, G Fiermonte, et al.
European Journal of Histochemistry : EJH|January 1, 1997
Evolution of chromosome Y in primatesM Rocchi, C T Storlazzi, R Marzella, et al.
Molecular and Cellular Probes|October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseasesP Gasparini, A Grifa, P Origone, et al.
Genomics|December 15, 1996
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19P Finelli, R Antonacci, R Marzella, et al.
Human Genetics|September 1, 1986
Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9M Rocchi, L Roncuzzi, R Santamaria, et al.
Cancer Genetics and Cytogenetics|May 9, 2002
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastomaL Sainati, A Leszl, C Surace, et al.
American Journal of Medical Genetics|May 1, 1983
Brief report: linkage between G6PD and fragile-X syndromeG Filippi, A Rinaldi, N Archidiacono, et al.
Pageof 31

Showing results (91-100 of 309) with videos related to

Sort By:
Pageof 31
Genomics|January 20, 1995
Comparative mapping of human alphoid sequences in great apes using fluorescence in situ hybridizationN Archidiacono, R Antonacci, R Marzella, et al.
Advances in Neurology|January 1, 1988
X-linked muscular dystrophies: studies through functional assay and DNA polymorphismsG Romeo, M Rocchi, L Roncuzzi, et al.
Prenatal Diagnosis|May 1, 1985
Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytesM Rocchi, V Pecile, N Archidiacono, et al.
Cytogenetics and Cell Genetics|July 28, 2001
Genomic organization and mapping of the gene (SLC25A19) encoding the human mitochondrial deoxynucleotide carrier (DNC)V Iacobazzi, M Ventura, G Fiermonte, et al.
European Journal of Histochemistry : EJH|January 1, 1997
Evolution of chromosome Y in primatesM Rocchi, C T Storlazzi, R Marzella, et al.
Molecular and Cellular Probes|October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseasesP Gasparini, A Grifa, P Origone, et al.
Genomics|December 15, 1996
Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19P Finelli, R Antonacci, R Marzella, et al.
Human Genetics|September 1, 1986
Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9M Rocchi, L Roncuzzi, R Santamaria, et al.
Cancer Genetics and Cytogenetics|May 9, 2002
Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastomaL Sainati, A Leszl, C Surace, et al.
American Journal of Medical Genetics|May 1, 1983
Brief report: linkage between G6PD and fragile-X syndromeG Filippi, A Rinaldi, N Archidiacono, et al.
Pageof 31