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G Novelli

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Genomics|April 1, 1991
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosisF Sangiuolo, G Novelli, S Murru, et al.
Prenatal Diagnosis|May 1, 1987
First trimester studies of a fetus at risk for triose phosphate isomerase deficiencyB Dallapiccola, G Novelli, C Cuoco, et al.
Neurogenetics|May 1, 1997
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variationG Novelli, S Semprini, F Capon, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 1, 1996
[Genetic aspects of deafness]B Dallapiccola, R Mingarelli, M Gennarelli, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1987
Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear familiesG Novelli, L Potenza, A Ruzzo, et al.
Minerva Ginecologica|January 1, 1981
[Cytological and endocrinological observations in fallopian tube carcinoma]G G Novelli, F Piovesan, F Borruto, et al.
Pharmacogenomics|March 22, 2001
Pharmacogenetics of human androgens and prostatic diseasesG Novelli, K Margiotti, F Sangiuolo, et al.
PCR Methods and Applications|December 1, 1993
PCR protocol for DNA recovery from Spurr's-embedded muscle biopsiesF Capon, S L Cicero, G Novelli, et al.
Gene Therapy|May 29, 2002
Genome medicine: gene therapy for the millennium, 30 September-3 October 2001, Rome, ItalyD C Gruenert, G Novelli, B Dallapiccola, et al.
Minerva Ginecologica|March 1, 1980
[Critical evaluation of hysterography after cesarean section]G Milani, G G Novelli, L Zanoio, et al.
Pageof 33

Showing results (41-50 of 330) with videos related to

Sort By:
Pageof 33
Genomics|April 1, 1991
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosisF Sangiuolo, G Novelli, S Murru, et al.
Prenatal Diagnosis|May 1, 1987
First trimester studies of a fetus at risk for triose phosphate isomerase deficiencyB Dallapiccola, G Novelli, C Cuoco, et al.
Neurogenetics|May 1, 1997
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variationG Novelli, S Semprini, F Capon, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 1, 1996
[Genetic aspects of deafness]B Dallapiccola, R Mingarelli, M Gennarelli, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1987
Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear familiesG Novelli, L Potenza, A Ruzzo, et al.
Minerva Ginecologica|January 1, 1981
[Cytological and endocrinological observations in fallopian tube carcinoma]G G Novelli, F Piovesan, F Borruto, et al.
Pharmacogenomics|March 22, 2001
Pharmacogenetics of human androgens and prostatic diseasesG Novelli, K Margiotti, F Sangiuolo, et al.
PCR Methods and Applications|December 1, 1993
PCR protocol for DNA recovery from Spurr's-embedded muscle biopsiesF Capon, S L Cicero, G Novelli, et al.
Gene Therapy|May 29, 2002
Genome medicine: gene therapy for the millennium, 30 September-3 October 2001, Rome, ItalyD C Gruenert, G Novelli, B Dallapiccola, et al.
Minerva Ginecologica|March 1, 1980
[Critical evaluation of hysterography after cesarean section]G Milani, G G Novelli, L Zanoio, et al.
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