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L Felicetti

Showing results (31-40 of 42) with videos related to

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American Journal of Human Genetics|June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophyS Cacurri, N Piazzo, G Deidda, et al.
American Journal of Human Genetics|November 1, 1986
Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypesA Di Rienzo, A Novelletto, M C Aliquò, et al.
The Open Dentistry Journal|December 18, 2008
Predictive Role of p53 Protein as a Single Marker or Associated to Ki67 Antigen in Oral CarcinogenesisL Montebugnoli, L Felicetti, D B Gissi, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
American Journal of Hematology|June 1, 1995
Sickle cell anemia and beta-gene cluster haplotypes in CubaA Muniz, L Corral, C Alaez, et al.
Western Journal of Nursing Research|June 25, 2016
Patient-Centered Participatory Research in Three Health Clinics: Benefits, Challenges, and Lessons LearnedNicole M Fava, Michelle L Munro-Kramer, Irene L Felicetti, et al.
Human Genetics|August 1, 1990
Molecular characterization of beta-thalassemia mutations in EgyptA Novelletto, M Hafez, G Deidda, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1994
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative studyF Mioni, G A Danieli, A Cao, et al.
Human Genetics|February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in EgyptA Novelletto, M Hafez, A Di Rienzo, et al.
Neuromuscular Disorders : NMD|December 9, 2003
Changes in motor cortex excitability in facioscapulohumeral muscular dystrophyV Di Lazzaro, A Oliviero, P A Tonali, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophyS Cacurri, N Piazzo, G Deidda, et al.
American Journal of Human Genetics|November 1, 1986
Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypesA Di Rienzo, A Novelletto, M C Aliquò, et al.
The Open Dentistry Journal|December 18, 2008
Predictive Role of p53 Protein as a Single Marker or Associated to Ki67 Antigen in Oral CarcinogenesisL Montebugnoli, L Felicetti, D B Gissi, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
American Journal of Hematology|June 1, 1995
Sickle cell anemia and beta-gene cluster haplotypes in CubaA Muniz, L Corral, C Alaez, et al.
Western Journal of Nursing Research|June 25, 2016
Patient-Centered Participatory Research in Three Health Clinics: Benefits, Challenges, and Lessons LearnedNicole M Fava, Michelle L Munro-Kramer, Irene L Felicetti, et al.
Human Genetics|August 1, 1990
Molecular characterization of beta-thalassemia mutations in EgyptA Novelletto, M Hafez, G Deidda, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1994
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative studyF Mioni, G A Danieli, A Cao, et al.
Human Genetics|February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in EgyptA Novelletto, M Hafez, A Di Rienzo, et al.
Neuromuscular Disorders : NMD|December 9, 2003
Changes in motor cortex excitability in facioscapulohumeral muscular dystrophyV Di Lazzaro, A Oliviero, P A Tonali, et al.
Pageof 5