Search research articles
Contact Us
Filters
Showing results (11-20 of 117) with videos related to
Page
of 12
Sort By:
Human Genetics
|
November 1, 1989
Haplotype frequencies of the collagen type-I genes in the Italian population
M Mottes, L Cugola, P F Pignatti
Molecular and Cellular Probes
|
June 17, 1999
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA
S Mirandola, P F Pignatti, M Mottes
Molecular and Cellular Probes
|
November 25, 2000
Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta
S Mirandola, P F Pignatti, M Mottes
Molecular and Cellular Probes
|
February 1, 1993
Genetic variation in the Italian population at five tandem repeat loci amplified in vitro: use in paternity testing
E Trabetti, R Galavotti, P F Pignatti
Journal of Virology
|
January 1, 1975
Chromatin-like structures in polyoma virus and simian virus 10 lytic cycle
C Cremisi, P F Pignatti, O Croissant, et al.
Molecular and Cellular Probes
|
February 1, 1992
Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations
P Gasparini, A Bonizzato, M Dognini, et al.
Journal of Medical Genetics
|
June 1, 1990
Segregation analysis of dominant osteogenesis imperfecta in Italy
M Mottes, L Cugola, N Cappello, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1978
Minichromosome from BK virus as a template for transcription in vitro
G Meneguzzi, P F Pignatti, G Barbanti-Brodano, et al.
Molecular and Cellular Probes
|
June 1, 1996
Intrafamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene
L Cohen-Solal, F Zolezzi, P F Pignatti, et al.
Clinical Genetics
|
October 1, 1991
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families
A Turco, B Peissel, L Gammaro, et al.
Page
of 12
Search research articles
Search
Showing results (11-20 of 117) with videos related to
Sort By:
Page
of 12
Human Genetics
|
November 1, 1989
Haplotype frequencies of the collagen type-I genes in the Italian population
M Mottes, L Cugola, P F Pignatti
Molecular and Cellular Probes
|
June 17, 1999
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA
S Mirandola, P F Pignatti, M Mottes
Molecular and Cellular Probes
|
November 25, 2000
Three novel polymorphic sequence variants in the type I collagen gene COL1A1, the main disease locus for Osteogenesis Imperfecta
S Mirandola, P F Pignatti, M Mottes
Molecular and Cellular Probes
|
February 1, 1993
Genetic variation in the Italian population at five tandem repeat loci amplified in vitro: use in paternity testing
E Trabetti, R Galavotti, P F Pignatti
Journal of Virology
|
January 1, 1975
Chromatin-like structures in polyoma virus and simian virus 10 lytic cycle
C Cremisi, P F Pignatti, O Croissant, et al.
Molecular and Cellular Probes
|
February 1, 1992
Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutations
P Gasparini, A Bonizzato, M Dognini, et al.
Journal of Medical Genetics
|
June 1, 1990
Segregation analysis of dominant osteogenesis imperfecta in Italy
M Mottes, L Cugola, N Cappello, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1978
Minichromosome from BK virus as a template for transcription in vitro
G Meneguzzi, P F Pignatti, G Barbanti-Brodano, et al.
Molecular and Cellular Probes
|
June 1, 1996
Intrafamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 gene
L Cohen-Solal, F Zolezzi, P F Pignatti, et al.
Clinical Genetics
|
October 1, 1991
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families
A Turco, B Peissel, L Gammaro, et al.
Page
of 12