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G Novelli

Showing results (141-150 of 330) with videos related to

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American Journal of Human Genetics|July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22M Mangino, O Sanchez, I Torrente, et al.
Molecular and Cellular Probes|April 1, 1995
Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patientsC Férec, G Novelli, C Verlingue, et al.
Human Mutation|January 1, 1996
Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiencyP Maceratesi, F Sangiuolo, G Novelli, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|March 12, 2008
Giant hemangiomas of the liver: surgical strategies and technical aspectsP Berloco, P Bruzzone, G Mennini, et al.
Cell Biochemistry and Function|September 1, 1993
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) geneG Novelli, M Gennarelli, F Sangiuolo, et al.
Molecular and Cellular Probes|June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patientsF Capon, S Melchionda, M Gennarelli, et al.
Cell Biochemistry and Function|December 1, 1992
Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscleG Novelli, M Gennarelli, G Zelano, et al.
Journal of Endocrinological Investigation|October 13, 2005
Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: response to 12-month triiodothyroacetic acid (TRIAC) therapyP Torre, M Bertoli, S Di Giovanni, et al.
La Clinica Terapeutica|July 7, 2007
[New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases]G Novelli, R Mango, L Vecchione, et al.
Pageof 33

Showing results (141-150 of 330) with videos related to

Sort By:
Pageof 33
American Journal of Human Genetics|July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22M Mangino, O Sanchez, I Torrente, et al.
Molecular and Cellular Probes|April 1, 1995
Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patientsC Férec, G Novelli, C Verlingue, et al.
Human Mutation|January 1, 1996
Three new mutations (P183T, V150L, 528insG) and eleven sequence polymorphisms in Italian patients with galactose-1-phosphate uridyltransferase (GALT) deficiencyP Maceratesi, F Sangiuolo, G Novelli, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
HPB : the Official Journal of the International Hepato Pancreato Biliary Association|March 12, 2008
Giant hemangiomas of the liver: surgical strategies and technical aspectsP Berloco, P Bruzzone, G Mennini, et al.
Cell Biochemistry and Function|September 1, 1993
Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) geneG Novelli, M Gennarelli, F Sangiuolo, et al.
Molecular and Cellular Probes|June 1, 1993
A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patientsF Capon, S Melchionda, M Gennarelli, et al.
Cell Biochemistry and Function|December 1, 1992
Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscleG Novelli, M Gennarelli, G Zelano, et al.
Journal of Endocrinological Investigation|October 13, 2005
Endocrine and neuropsychological assessment in a child with a novel mutation of thyroid hormone receptor: response to 12-month triiodothyroacetic acid (TRIAC) therapyP Torre, M Bertoli, S Di Giovanni, et al.
La Clinica Terapeutica|July 7, 2007
[New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases]G Novelli, R Mango, L Vecchione, et al.
Pageof 33