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M Rocchi

Showing results (151-160 of 309) with videos related to

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Cytogenetics and Cell Genetics|June 1, 2000
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3F Vitelli, I Meloni, S Fineschi, et al.
Gene|October 6, 2001
Characterization of a highly repeated DNA sequence family in five species of the genus EulemurM Ventura, M Boniotto, M F Cardone, et al.
Genomics|July 1, 1994
Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12P Mandich, A M Schito, E Bellone, et al.
Genomics|February 28, 1998
PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/CJ Berthelsen, L Viggiano, H Schulz, et al.
Biochimica Et Biophysica Acta|October 19, 1999
The human gene coding for HCN2, a pacemaker channel of the heartT Vaccari, A Moroni, M Rocchi, et al.
Pacing and Clinical Electrophysiology : PACE|March 1, 1980
Possible risks of general anesthesia in patients with intraventricular conduction disturbancesM Santini, P Carrara, M Benhar, et al.
Journal of Medical Genetics|May 2, 2006
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architectureR Ciccone, T Mattina, R Giorda, et al.
Human Genetics|February 1, 1993
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13A Baldini, T Ried, V Shridhar, et al.
Cytogenetics and Cell Genetics|January 1, 1997
A panel of radiation hybrids and YAC clones specific for human chromosome 5R Marzella, L Viggiano, A S Ricco, et al.
Indian Journal of Cancer|January 13, 2004
Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignanciesV J Frenny, Z Antonella, A Luisa, et al.
Pageof 31

Showing results (151-160 of 309) with videos related to

Sort By:
Pageof 31
Cytogenetics and Cell Genetics|June 1, 2000
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3F Vitelli, I Meloni, S Fineschi, et al.
Gene|October 6, 2001
Characterization of a highly repeated DNA sequence family in five species of the genus EulemurM Ventura, M Boniotto, M F Cardone, et al.
Genomics|July 1, 1994
Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12P Mandich, A M Schito, E Bellone, et al.
Genomics|February 28, 1998
PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/CJ Berthelsen, L Viggiano, H Schulz, et al.
Biochimica Et Biophysica Acta|October 19, 1999
The human gene coding for HCN2, a pacemaker channel of the heartT Vaccari, A Moroni, M Rocchi, et al.
Pacing and Clinical Electrophysiology : PACE|March 1, 1980
Possible risks of general anesthesia in patients with intraventricular conduction disturbancesM Santini, P Carrara, M Benhar, et al.
Journal of Medical Genetics|May 2, 2006
Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architectureR Ciccone, T Mattina, R Giorda, et al.
Human Genetics|February 1, 1993
An alphoid DNA sequence conserved in all human and great ape chromosomes: evidence for ancient centromeric sequences at human chromosomal regions 2q21 and 9q13A Baldini, T Ried, V Shridhar, et al.
Cytogenetics and Cell Genetics|January 1, 1997
A panel of radiation hybrids and YAC clones specific for human chromosome 5R Marzella, L Viggiano, A S Ricco, et al.
Indian Journal of Cancer|January 13, 2004
Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignanciesV J Frenny, Z Antonella, A Luisa, et al.
Pageof 31