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Human Mutation
|
March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCR
J Purroy, L Bisceglia, J Jaeken, et al.
Journal of Medical Genetics
|
August 27, 1998
Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family
P Gasparini, A De Fazio, A I Croce, et al.
Recenti Progressi in Medicina
|
March 1, 1994
[Immune hemolytic anemia and acute kidney failure due to rifampicin]
F Guzzini, F Angiolini, L Cazzaniga, et al.
Journal of Internal Medicine
|
March 1, 1992
Prevalence of hyperinsulinaemia in patients with high blood pressure
I Zavaroni, S Mazza, E Dall'Aglio, et al.
American Journal of Medical Genetics. Part A
|
January 8, 2005
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactyly
C Vitiello, P D'Adamo, F Gentile, et al.
The American Journal of Cardiology
|
May 1, 1994
Cigarette smokers are relatively glucose intolerant, hyperinsulinemic and dyslipidemic
I Zavaroni, L Bonini, P Gasparini, et al.
Bone Marrow Transplantation
|
December 1, 1989
Bone marrow transplantation monitoring by DNA analysis
P Gasparini, G Martinelli, E Trabetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
Can weight gain in healthy, nonobese volunteers be predicted by differences in baseline plasma insulin concentration?
I Zavaroni, A Zuccarelli, P Gasparini, et al.
Human Genetics
|
September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families
G Novelli, P Gasparini, A Savoia, et al.
European Journal of Pediatrics
|
December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort study
G Borgo, P Gasparini, A Bonizzato, et al.
Page
of 21
Search research articles
Search
Showing results (51-60 of 204) with videos related to
Sort By:
Page
of 21
Human Mutation
|
March 29, 2000
Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCR
J Purroy, L Bisceglia, J Jaeken, et al.
Journal of Medical Genetics
|
August 27, 1998
Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family
P Gasparini, A De Fazio, A I Croce, et al.
Recenti Progressi in Medicina
|
March 1, 1994
[Immune hemolytic anemia and acute kidney failure due to rifampicin]
F Guzzini, F Angiolini, L Cazzaniga, et al.
Journal of Internal Medicine
|
March 1, 1992
Prevalence of hyperinsulinaemia in patients with high blood pressure
I Zavaroni, S Mazza, E Dall'Aglio, et al.
American Journal of Medical Genetics. Part A
|
January 8, 2005
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactyly
C Vitiello, P D'Adamo, F Gentile, et al.
The American Journal of Cardiology
|
May 1, 1994
Cigarette smokers are relatively glucose intolerant, hyperinsulinemic and dyslipidemic
I Zavaroni, L Bonini, P Gasparini, et al.
Bone Marrow Transplantation
|
December 1, 1989
Bone marrow transplantation monitoring by DNA analysis
P Gasparini, G Martinelli, E Trabetti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
Can weight gain in healthy, nonobese volunteers be predicted by differences in baseline plasma insulin concentration?
I Zavaroni, A Zuccarelli, P Gasparini, et al.
Human Genetics
|
September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families
G Novelli, P Gasparini, A Savoia, et al.
European Journal of Pediatrics
|
December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort study
G Borgo, P Gasparini, A Bonizzato, et al.
Page
of 21