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O Zuffardi

Showing results (91-100 of 159) with videos related to

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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.
Genomics|August 1, 1996
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)N Mastroianni, M De Fusco, M Zollo, et al.
Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Clinical Genetics|November 1, 1986
A new chromosome instability disorderP Maraschio, D Peretti, S Lambiase, et al.
Genomics|February 28, 1998
Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genesM Rocchigiani, M Lestingi, A Luddi, et al.
Human Genetics|April 1, 1989
Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?O Zuffardi, A Caiulo, P Maraschio, et al.
Human Genetics|February 1, 1991
Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23A Caiulo, S Nicolis, P Bianchi, et al.
Genomics|November 1, 1994
Order of six loci at 2q24-q31 and orientation of the HOXD locusE Rossi, A Faiella, M Zeviani, et al.
Human Genetics|June 1, 1997
Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?M Piantanida, C Dellavecchia, G Floridia, et al.
Pageof 16

Showing results (91-100 of 159) with videos related to

Sort By:
Pageof 16
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.
Genomics|August 1, 1996
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)N Mastroianni, M De Fusco, M Zollo, et al.
Acta Anthropogenetica|January 1, 1983
H-Y antigen in human X-autosome translocationsA Mayerova, O Zuffardi, P Maraschio, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
Clinical Genetics|November 1, 1986
A new chromosome instability disorderP Maraschio, D Peretti, S Lambiase, et al.
Genomics|February 28, 1998
Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genesM Rocchigiani, M Lestingi, A Luddi, et al.
Human Genetics|April 1, 1989
Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?O Zuffardi, A Caiulo, P Maraschio, et al.
Human Genetics|February 1, 1991
Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23A Caiulo, S Nicolis, P Bianchi, et al.
Genomics|November 1, 1994
Order of six loci at 2q24-q31 and orientation of the HOXD locusE Rossi, A Faiella, M Zeviani, et al.
Human Genetics|June 1, 1997
Ataxic gait and mental retardation with absence of the paternal chromosome 8 and an idic(8)(p23.3): imprinting effect or nullisomy for distal 8p genes?M Piantanida, C Dellavecchia, G Floridia, et al.
Pageof 16