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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
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January 1, 1993
Plasmid DNA and low-frequency electromagnetic fields
L D'Agruma, A Colosimo, U Angeloni, et al.
Human Genetics
|
April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms
P Gasparini, L D'Agruma, G Pio de Cillis, 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) gene
G Novelli, M Gennarelli, F Sangiuolo, et al.
Annals of Neurology
|
February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
V Tiranti, L D'Agruma, D Pareyson, et al.
Human Genetics
|
September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
R Rabionet, L Zelante, N López-Bigas, et al.
British Journal of Haematology
|
December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background
S Perrotta, M D Cappellini, F Bertoldo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 26, 2000
Transforming growth factor-beta1 gene polymorphism, bone turnover, and bone mass in Italian postmenopausal women
F Bertoldo, L D'Agruma, F Furlan, et al.
Human Genetics
|
April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)
A Totaro, A Grifa, A Roetto, et al.
Cellular Oncology (Dordrecht, Netherlands)
|
August 13, 2014
A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome
M G Chiofalo, A Sparaneo, M Chetta, et al.
Lancet (London, England)
|
March 3, 1998
Connexin-26 mutations in sporadic and inherited sensorineural deafness
X Estivill, P Fortina, S Surrey, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1993
Plasmid DNA and low-frequency electromagnetic fields
L D'Agruma, A Colosimo, U Angeloni, et al.
Human Genetics
|
April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms
P Gasparini, L D'Agruma, G Pio de Cillis, 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) gene
G Novelli, M Gennarelli, F Sangiuolo, et al.
Annals of Neurology
|
February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
V Tiranti, L D'Agruma, D Pareyson, et al.
Human Genetics
|
September 12, 2000
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
R Rabionet, L Zelante, N López-Bigas, et al.
British Journal of Haematology
|
December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic background
S Perrotta, M D Cappellini, F Bertoldo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 26, 2000
Transforming growth factor-beta1 gene polymorphism, bone turnover, and bone mass in Italian postmenopausal women
F Bertoldo, L D'Agruma, F Furlan, et al.
Human Genetics
|
April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)
A Totaro, A Grifa, A Roetto, et al.
Cellular Oncology (Dordrecht, Netherlands)
|
August 13, 2014
A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome
M G Chiofalo, A Sparaneo, M Chetta, et al.
Lancet (London, England)
|
March 3, 1998
Connexin-26 mutations in sporadic and inherited sensorineural deafness
X Estivill, P Fortina, S Surrey, et al.
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of 2