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M Rocchi

Showing results (181-190 of 309) with videos related to

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American Journal of Medical Genetics|July 12, 1996
+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markersR Robledo, P Melis, M Siniscalco, et al.
Human Genetics|June 1, 1989
Assignment of human aldolase C gene to chromosome 17, region cen----q21.1M Rocchi, E Vitale, A Covone, et al.
Somatic Cell and Molecular Genetics|September 1, 1994
Cloning and comparative mapping of recently evolved human chromosome 22-specific alpha satellite DNAM Rocchi, N Archidiacono, R Antonacci, et al.
Human Genetics|March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomesP Maraschio, R Tupler, E Rossi, et al.
British Journal of Haematology|May 8, 1999
A novel translocation t(1;7)(p36;q34) in three patients with acute myeloid leukaemiaG Specchia, A Cuneo, V Liso, et al.
American Journal of Medical Genetics|September 15, 1991
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutationsG Filippi, A Arslanian, F Dagna-Bricarelli, et al.
Human Molecular Genetics|November 11, 1999
Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural developmentM Mariani, D Baldessari, S Francisconi, et al.
Genomics|January 20, 1995
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.
The Journal of Small Animal Practice|May 12, 2015
Pneumopericardium, pneumomediastinum, pneumothorax and pneumoretroperitoneum complicating pulmonary metastatic carcinoma in a catV Greci, A Baio, L Bibbiani, et al.
Annals of Hematology|June 13, 2001
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant caseG Specchia, C T Storlazzi, A Cuneo, et al.
Pageof 31

Showing results (181-190 of 309) with videos related to

Sort By:
Pageof 31
American Journal of Medical Genetics|July 12, 1996
+2.71 LOD score at zero recombination is not sufficient for establishing linkage between X-linked mental retardation and X-chromosome markersR Robledo, P Melis, M Siniscalco, et al.
Human Genetics|June 1, 1989
Assignment of human aldolase C gene to chromosome 17, region cen----q21.1M Rocchi, E Vitale, A Covone, et al.
Somatic Cell and Molecular Genetics|September 1, 1994
Cloning and comparative mapping of recently evolved human chromosome 22-specific alpha satellite DNAM Rocchi, N Archidiacono, R Antonacci, et al.
Human Genetics|March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomesP Maraschio, R Tupler, E Rossi, et al.
British Journal of Haematology|May 8, 1999
A novel translocation t(1;7)(p36;q34) in three patients with acute myeloid leukaemiaG Specchia, A Cuneo, V Liso, et al.
American Journal of Medical Genetics|September 15, 1991
Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutationsG Filippi, A Arslanian, F Dagna-Bricarelli, et al.
Human Molecular Genetics|November 11, 1999
Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural developmentM Mariani, D Baldessari, S Francisconi, et al.
Genomics|January 20, 1995
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.
The Journal of Small Animal Practice|May 12, 2015
Pneumopericardium, pneumomediastinum, pneumothorax and pneumoretroperitoneum complicating pulmonary metastatic carcinoma in a catV Greci, A Baio, L Bibbiani, et al.
Annals of Hematology|June 13, 2001
Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant caseG Specchia, C T Storlazzi, A Cuneo, et al.
Pageof 31