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Current Opinion in Hematology
|
March 1, 1996
Advances in molecular diagnosis of inherited hemoglobin disorders
P Sutcharitchan, S H Embury
Blood
|
November 1, 1986
Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene
M H Steinberg, S H Embury
Birth Defects Original Article Series
|
January 1, 1987
Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene
M H Steinberg, S H Embury
The Journal of Laboratory and Clinical Medicine
|
July 1, 1985
Monovalent cation changes in sickle erythrocytes: a direct reflection of alpha-globin gene number
S H Embury, K Backer, B E Glader
Blood
|
May 15, 1989
Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation
G L Kropp, S Fucharoen, S H Embury
Blood
|
July 1, 1991
Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation
G L Kropp, S Fucharoen, S H Embury
The Western Journal of Medicine
|
November 1, 1981
Risk of altitude exposure in sickle cell disease
S Claster, M J Godwin, S H Embury
Transactions of the Association of American Physicians
|
January 1, 1979
The frequent occurrence of alpha thalassemia in blacks
A M Dozy, S H Embury, Y W Kan
Annals of the New York Academy of Sciences
|
January 1, 1980
Molecular mechanisms in alpha thalassemia: racial differences in alpha-globin gene organization
S H Embury, A M Dozy, Y W Kan
American Journal of Hematology
|
January 1, 1988
Oxygen-induced marrow red cell hypoplasia leading to transfusion in sickle painful crisis
P K Lane, S H Embury, P T Toy
Page
of 6
Search research articles
Search
Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Current Opinion in Hematology
|
March 1, 1996
Advances in molecular diagnosis of inherited hemoglobin disorders
P Sutcharitchan, S H Embury
Blood
|
November 1, 1986
Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene
M H Steinberg, S H Embury
Birth Defects Original Article Series
|
January 1, 1987
Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene
M H Steinberg, S H Embury
The Journal of Laboratory and Clinical Medicine
|
July 1, 1985
Monovalent cation changes in sickle erythrocytes: a direct reflection of alpha-globin gene number
S H Embury, K Backer, B E Glader
Blood
|
May 15, 1989
Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation
G L Kropp, S Fucharoen, S H Embury
Blood
|
July 1, 1991
Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation
G L Kropp, S Fucharoen, S H Embury
The Western Journal of Medicine
|
November 1, 1981
Risk of altitude exposure in sickle cell disease
S Claster, M J Godwin, S H Embury
Transactions of the Association of American Physicians
|
January 1, 1979
The frequent occurrence of alpha thalassemia in blacks
A M Dozy, S H Embury, Y W Kan
Annals of the New York Academy of Sciences
|
January 1, 1980
Molecular mechanisms in alpha thalassemia: racial differences in alpha-globin gene organization
S H Embury, A M Dozy, Y W Kan
American Journal of Hematology
|
January 1, 1988
Oxygen-induced marrow red cell hypoplasia leading to transfusion in sickle painful crisis
P K Lane, S H Embury, P T Toy
Page
of 6