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G Novelli

Showing results (91-100 of 330) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1997
Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 geneA Botta, V Jurecic, A Pizzuti, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at riskM P Iampieri, R Mingarelli, E Le Guern, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 10, 2001
Targeted correction of a defective selectable marker gene in human epithelial cells by small DNA fragmentsA Colosimo, K K Goncz, G Novelli, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3F Sangiuolo, E Bruscia, F Capon, et al.
American Journal of Human Genetics|April 1, 1992
The cystic fibrosis delta F508 mutation in the Albanian populationG Novelli, F Sangiuolo, V Mokini, et al.
The British Journal of Dermatology|January 3, 2013
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patientsT Lepre, R Cascella, M Ragazzo, et al.
Cell Biochemistry and Function|June 24, 1998
Genomic instability associated with myotonic dystrophy does not involve p53 expression and activityM Gennarelli, M Lucarelli, P Amicucci, et al.
Clinical Genetics|June 18, 1998
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical regionA Mari, F Amati, E Conti, et al.
Biochemical and Biophysical Research Communications|July 16, 1985
Increased rate of superoxide ion generation in Fanconi anemia erythrocytesM Scarpa, A Rigo, F Momo, et al.
Genetic Testing|May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophyS Semprini, A Tacconelli, F Capon, et al.
Pageof 33

Showing results (91-100 of 330) with videos related to

Sort By:
Pageof 33
Cytogenetics and Cell Genetics|January 1, 1997
Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 geneA Botta, V Jurecic, A Pizzuti, et al.
Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at riskM P Iampieri, R Mingarelli, E Le Guern, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 10, 2001
Targeted correction of a defective selectable marker gene in human epithelial cells by small DNA fragmentsA Colosimo, K K Goncz, G Novelli, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3F Sangiuolo, E Bruscia, F Capon, et al.
American Journal of Human Genetics|April 1, 1992
The cystic fibrosis delta F508 mutation in the Albanian populationG Novelli, F Sangiuolo, V Mokini, et al.
The British Journal of Dermatology|January 3, 2013
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patientsT Lepre, R Cascella, M Ragazzo, et al.
Cell Biochemistry and Function|June 24, 1998
Genomic instability associated with myotonic dystrophy does not involve p53 expression and activityM Gennarelli, M Lucarelli, P Amicucci, et al.
Clinical Genetics|June 18, 1998
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical regionA Mari, F Amati, E Conti, et al.
Biochemical and Biophysical Research Communications|July 16, 1985
Increased rate of superoxide ion generation in Fanconi anemia erythrocytesM Scarpa, A Rigo, F Momo, et al.
Genetic Testing|May 5, 2001
A single strand conformation polymorphism-based carrier test for spinal muscular atrophyS Semprini, A Tacconelli, F Capon, et al.
Pageof 33