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G Novelli

Showing results (31-40 of 330) with videos related to

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Minerva Ginecologica|April 1, 1980
[Preliminary endocrinological observations in menopausal patients under treatment with human chorionic gonadotropins (HCG)]G G Novelli, R Patton, F Piovesan
Journal of Neurology|January 1, 1996
Molecular basis of galactose-1-phosphate uridyltransferase deficiency involving skeletal muscleP Ninfali, N Bresolin, B Dallapiccola, et al.
International Journal of Clinical & Laboratory Research|January 1, 1996
Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassayA Colosimo, G Novelli, A Cavicchini, et al.
American Journal of Human Genetics|December 1, 1999
Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21F Capon, S Semprini, B Dallapiccola, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
The up-to-date molecular genetics of cystic fibrosisG Novelli, F Sangiuolo, P Maceratesi, et al.
Acta Haematologica|January 1, 1984
Increased activity of glutathione S-transferase and fast decay of reduced glutathione in Fanconi's anemia erythrocytesB Dallapiccola, M Magnani, G Novelli, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1997
From genetic research into clinical practiceB Dallapiccola, I Torrente, R Mingarelli, et al.
Human Genetics|March 1, 1992
Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reactionG Novelli, M Gennarelli, M Rocchi, et al.
American Journal of Medical Genetics|September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patientC Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry|February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasmaP Amicucci, M Gennarelli, G Novelli, et al.
Pageof 33

Showing results (31-40 of 330) with videos related to

Sort By:
Pageof 33
Minerva Ginecologica|April 1, 1980
[Preliminary endocrinological observations in menopausal patients under treatment with human chorionic gonadotropins (HCG)]G G Novelli, R Patton, F Piovesan
Journal of Neurology|January 1, 1996
Molecular basis of galactose-1-phosphate uridyltransferase deficiency involving skeletal muscleP Ninfali, N Bresolin, B Dallapiccola, et al.
International Journal of Clinical & Laboratory Research|January 1, 1996
Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassayA Colosimo, G Novelli, A Cavicchini, et al.
American Journal of Human Genetics|December 1, 1999
Evidence for interaction between psoriasis-susceptibility loci on chromosomes 6p21 and 1q21F Capon, S Semprini, B Dallapiccola, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
The up-to-date molecular genetics of cystic fibrosisG Novelli, F Sangiuolo, P Maceratesi, et al.
Acta Haematologica|January 1, 1984
Increased activity of glutathione S-transferase and fast decay of reduced glutathione in Fanconi's anemia erythrocytesB Dallapiccola, M Magnani, G Novelli, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1997
From genetic research into clinical practiceB Dallapiccola, I Torrente, R Mingarelli, et al.
Human Genetics|March 1, 1992
Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reactionG Novelli, M Gennarelli, M Rocchi, et al.
American Journal of Medical Genetics|September 20, 2000
Familial mandibuloacral dysplasia: report of an additional Italian patientC Tudisco, G Canepa, G Novelli, et al.
Clinical Chemistry|February 5, 2000
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasmaP Amicucci, M Gennarelli, G Novelli, et al.
Pageof 33