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American Journal of Medical Genetics
|
April 15, 1994
New variant of chromosome 11
V Aiello, N Ricci, P Palazzi, et al.
European Heart Journal
|
December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conduction
G Bosi, A Sensi, M Scorrano, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple method
F Gualandi, A Sensi, O Calabrese, et al.
Human Heredity
|
January 1, 1985
Human placental glucose dehydrogenase: IEF polymorphism in two Italian populations and enzyme activity in the six common phenotypes
R Scacchi, R M Corbo, E Calzolari, et al.
Journal of Medical Genetics
|
June 1, 1990
Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births
E Calzolari, D Manservigi, G P Garani, et al.
The Science of the Total Environment
|
May 16, 2000
Reproductive outcomes in a population exposed long-term to inorganic selenium via drinking water
M Vinceti, C I Cann, E Calzolari, et al.
Minerva Ginecologica
|
March 1, 1987
[Clinical experience of contraception in women over 40]
E Calzolari, G Perrone, D R Cazzato, et al.
Acta Neurologica Scandinavica
|
August 1, 1995
Expansion of a (CAG)n repeat region in a sporadic case of HD
A Bozza, S Malagù, E Calzolari, et al.
Drugs Under Experimental and Clinical Research
|
January 1, 1992
The efficacy of clarythromycin (A-56268, TE-031) in the treatment of genital chlamydial infection
E Calzolari, G Ciampaglia, M Steffe, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
P Prontera, A Sensi, G Pilu, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 135) with videos related to
Sort By:
Page
of 14
American Journal of Medical Genetics
|
April 15, 1994
New variant of chromosome 11
V Aiello, N Ricci, P Palazzi, et al.
European Heart Journal
|
December 1, 1995
Atrial septal defect type Ostium secundum with and without prolonged atrioventricular conduction
G Bosi, A Sensi, M Scorrano, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal exclusion of UPD from cytogenetic slides: a simple method
F Gualandi, A Sensi, O Calabrese, et al.
Human Heredity
|
January 1, 1985
Human placental glucose dehydrogenase: IEF polymorphism in two Italian populations and enzyme activity in the six common phenotypes
R Scacchi, R M Corbo, E Calzolari, et al.
Journal of Medical Genetics
|
June 1, 1990
Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births
E Calzolari, D Manservigi, G P Garani, et al.
The Science of the Total Environment
|
May 16, 2000
Reproductive outcomes in a population exposed long-term to inorganic selenium via drinking water
M Vinceti, C I Cann, E Calzolari, et al.
Minerva Ginecologica
|
March 1, 1987
[Clinical experience of contraception in women over 40]
E Calzolari, G Perrone, D R Cazzato, et al.
Acta Neurologica Scandinavica
|
August 1, 1995
Expansion of a (CAG)n repeat region in a sporadic case of HD
A Bozza, S Malagù, E Calzolari, et al.
Drugs Under Experimental and Clinical Research
|
January 1, 1992
The efficacy of clarythromycin (A-56268, TE-031) in the treatment of genital chlamydial infection
E Calzolari, G Ciampaglia, M Steffe, et al.
Genetic Counseling (Geneva, Switzerland)
|
March 23, 2007
FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
P Prontera, A Sensi, G Pilu, et al.
Page
of 14