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Journal of Endocrinological Investigation
|
May 1, 1997
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism
M Putzolu, A Meloni, S Loche, et al.
American Journal of Human Genetics
|
April 16, 1998
The -75A-->C substitution in the 5' UTR of the Wilson disease gene is a sequence polymorphism in the Mediterranean population
G Loudianos, V Dessi, M Lovicu, et al.
Annals of the New York Academy of Sciences
|
January 1, 1980
Prenatal diagnosis of beta thalassemia: experience with 133 cases and the effect of fetal blood sampling on child development
A Cao, M Furbetta, A Angius, et al.
Seminars in Hematology
|
January 1, 1996
Clinical experience of management of thalassemia: the Sardinian experience
A Cao, R Galanello, M C Rosatelli, et al.
Hemoglobin
|
January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemia
G Loudianos, P Moi, J Lavinha, et al.
Se Pu = Chinese Journal of Chromatography
|
May 1, 2001
[Determination of hyperin in Sanguisorba Officinalis L. by high performance liquid chromatography]
M Sha, A Cao, B Wang, et al.
Human Mutation
|
January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37
D Gasperini, L Perseu, P Cossu, et al.
Annals of Biomedical Engineering
|
August 29, 2019
In Vivo MRI Assessment of Blood Flow in Arteries and Veins from Head-to-Toe Across Age and Sex in C57BL/6 Mice
A Colleen Crouch, Amos A Cao, Ulrich M Scheven, et al.
Journal of Pediatric Orthopedics
|
February 9, 2022
Neuromuscular Patients Are 40% More Likely to Get a Cast Injury
Adrian J Lin, Lisa A Cao, Nina Lightdale-Miric, et al.
Genomics
|
May 1, 1990
Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A
S Murru, L Casula, M Pecorara, et al.
Page
of 47
Search research articles
Search
Showing results (141-150 of 461) with videos related to
Sort By:
Page
of 47
Journal of Endocrinological Investigation
|
May 1, 1997
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism
M Putzolu, A Meloni, S Loche, et al.
American Journal of Human Genetics
|
April 16, 1998
The -75A-->C substitution in the 5' UTR of the Wilson disease gene is a sequence polymorphism in the Mediterranean population
G Loudianos, V Dessi, M Lovicu, et al.
Annals of the New York Academy of Sciences
|
January 1, 1980
Prenatal diagnosis of beta thalassemia: experience with 133 cases and the effect of fetal blood sampling on child development
A Cao, M Furbetta, A Angius, et al.
Seminars in Hematology
|
January 1, 1996
Clinical experience of management of thalassemia: the Sardinian experience
A Cao, R Galanello, M C Rosatelli, et al.
Hemoglobin
|
January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemia
G Loudianos, P Moi, J Lavinha, et al.
Se Pu = Chinese Journal of Chromatography
|
May 1, 2001
[Determination of hyperin in Sanguisorba Officinalis L. by high performance liquid chromatography]
M Sha, A Cao, B Wang, et al.
Human Mutation
|
January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37
D Gasperini, L Perseu, P Cossu, et al.
Annals of Biomedical Engineering
|
August 29, 2019
In Vivo MRI Assessment of Blood Flow in Arteries and Veins from Head-to-Toe Across Age and Sex in C57BL/6 Mice
A Colleen Crouch, Amos A Cao, Ulrich M Scheven, et al.
Journal of Pediatric Orthopedics
|
February 9, 2022
Neuromuscular Patients Are 40% More Likely to Get a Cast Injury
Adrian J Lin, Lisa A Cao, Nina Lightdale-Miric, et al.
Genomics
|
May 1, 1990
Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A
S Murru, L Casula, M Pecorara, et al.
Page
of 47