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American Journal of Human Genetics
|
September 1, 1976
Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type)
G Romeo, A Rinaldi, F Urbano, et al.
Biochemical Genetics
|
December 1, 1970
Uroporphyrinogen 3 cosynthetase in asymptomatic carriers of congenital erythpoietic porphyria
G Romeo, B L Glenn, E Y Levin
American Journal of Human Genetics
|
May 1, 1990
Analysis of delta F508 does not confirm a previously reported recombination in a cystic fibrosis family
M Devoto, P Ronchetto, L Romano, et al.
Minerva Chirurgica
|
April 15, 1991
[Intraoperative esophageal manometry]
G Romeo, G Beneventano, M Migliore, et al.
La Medicina Del Lavoro
|
August 1, 2014
[Multiple self-notifications in 2000-2001 of occupational diseases to the registration system MALPROF]
A Baldasseroni, Giulia Lubrano, G Romeo, et al.
Differentiation; Research in Biological Diversity
|
January 1, 1985
Subcellular distribution of 2',5'-oligoadenylate synthetase in differentiating Friend leukemia cells
N Mechti, E Affabris, G Romeo, et al.
American Journal of Medical Genetics
|
December 18, 1996
Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome
M Silengo, M Lerone, M Seri, et al.
Archives of Internal Medicine
|
May 1, 1970
Intra-arterial administration of reserpine. Its use in patients with Raynaud's disease or Raynaud's phenomenon
S G Romeo, R E Whalen, J P Tindall
Recenti Progressi in Medicina
|
December 1, 1990
[Bence-Jones proteinuria in multiple sclerosis: a possible indicator of disease activity]
E Pascali, A Pezzoli, G Romeo, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology
|
December 1, 1993
[Plasma malondialdehyde in patients with chronic renal insufficiency undergoing hemodialytic treatment]
C M Bruno, S Neri, C Spata, et al.
Page
of 57
Search research articles
Search
Showing results (71-80 of 565) with videos related to
Sort By:
Page
of 57
American Journal of Human Genetics
|
September 1, 1976
Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type)
G Romeo, A Rinaldi, F Urbano, et al.
Biochemical Genetics
|
December 1, 1970
Uroporphyrinogen 3 cosynthetase in asymptomatic carriers of congenital erythpoietic porphyria
G Romeo, B L Glenn, E Y Levin
American Journal of Human Genetics
|
May 1, 1990
Analysis of delta F508 does not confirm a previously reported recombination in a cystic fibrosis family
M Devoto, P Ronchetto, L Romano, et al.
Minerva Chirurgica
|
April 15, 1991
[Intraoperative esophageal manometry]
G Romeo, G Beneventano, M Migliore, et al.
La Medicina Del Lavoro
|
August 1, 2014
[Multiple self-notifications in 2000-2001 of occupational diseases to the registration system MALPROF]
A Baldasseroni, Giulia Lubrano, G Romeo, et al.
Differentiation; Research in Biological Diversity
|
January 1, 1985
Subcellular distribution of 2',5'-oligoadenylate synthetase in differentiating Friend leukemia cells
N Mechti, E Affabris, G Romeo, et al.
American Journal of Medical Genetics
|
December 18, 1996
Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome
M Silengo, M Lerone, M Seri, et al.
Archives of Internal Medicine
|
May 1, 1970
Intra-arterial administration of reserpine. Its use in patients with Raynaud's disease or Raynaud's phenomenon
S G Romeo, R E Whalen, J P Tindall
Recenti Progressi in Medicina
|
December 1, 1990
[Bence-Jones proteinuria in multiple sclerosis: a possible indicator of disease activity]
E Pascali, A Pezzoli, G Romeo, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology
|
December 1, 1993
[Plasma malondialdehyde in patients with chronic renal insufficiency undergoing hemodialytic treatment]
C M Bruno, S Neri, C Spata, et al.
Page
of 57