Search research articles
Contact Us
Filters
Showing results (61-70 of 73) with videos related to
Page
of 8
Sort By:
Archives of Internal Medicine
|
May 1, 1983
Iron deficiency and sickle cell anemia
K R Rao, A R Patel, G R Honig, et al.
Blood
|
November 1, 1974
Sickle hemoglobin in combination with HbJBangkok (alphaA2beta56-2gly leads to asp)
U Gunay, C Pauli, M Shamsuddin, et al.
American Journal of Obstetrics and Gynecology
|
November 15, 1983
Biphasic changes in hemoglobin A1c concentrations during normal human pregnancy
R L Phelps, G R Honig, D Green, et al.
Biochimica Et Biophysica Acta
|
December 16, 1980
Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity
G R Honig, L N Vida, M Shamsuddin, et al.
Blood
|
April 1, 1980
Two new sickle cell syndromes: HbS, Hb Camden, and alpha-thalassemia; and HbS in combination with Hb Tacoma
G R Honig, R G Mason, M Shamsuddin, et al.
American Journal of Human Genetics
|
September 1, 1982
The identification of fanconi anemia genotypes by clastogenic stress
M M Cohen, S J Simpson, G R Honig, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1980
Processing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia
L E Maquat, A J Kinniburgh, L R Beach, et al.
Biological Chemistry Hoppe-Seyler
|
October 1, 1985
The primary structure and functional properties of the hemoglobins of a ground squirrel (Spermophilus townsendii, Rodentia)
T Kleinschmidt, F A Bieber, C F Nadler, et al.
The Journal of Clinical Investigation
|
July 1, 1973
Hemoglobin Abraham Lincoln, beta32 (B14) leucine leads to proline. An unstable variant producing severe hemolytic disease
G R Honig, D Green, M Shamsuddin, et al.
Blood
|
January 1, 1980
Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia
G R Honig, M Shamsuddin, R G Mason, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 8
Archives of Internal Medicine
|
May 1, 1983
Iron deficiency and sickle cell anemia
K R Rao, A R Patel, G R Honig, et al.
Blood
|
November 1, 1974
Sickle hemoglobin in combination with HbJBangkok (alphaA2beta56-2gly leads to asp)
U Gunay, C Pauli, M Shamsuddin, et al.
American Journal of Obstetrics and Gynecology
|
November 15, 1983
Biphasic changes in hemoglobin A1c concentrations during normal human pregnancy
R L Phelps, G R Honig, D Green, et al.
Biochimica Et Biophysica Acta
|
December 16, 1980
Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity
G R Honig, L N Vida, M Shamsuddin, et al.
Blood
|
April 1, 1980
Two new sickle cell syndromes: HbS, Hb Camden, and alpha-thalassemia; and HbS in combination with Hb Tacoma
G R Honig, R G Mason, M Shamsuddin, et al.
American Journal of Human Genetics
|
September 1, 1982
The identification of fanconi anemia genotypes by clastogenic stress
M M Cohen, S J Simpson, G R Honig, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1980
Processing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia
L E Maquat, A J Kinniburgh, L R Beach, et al.
Biological Chemistry Hoppe-Seyler
|
October 1, 1985
The primary structure and functional properties of the hemoglobins of a ground squirrel (Spermophilus townsendii, Rodentia)
T Kleinschmidt, F A Bieber, C F Nadler, et al.
The Journal of Clinical Investigation
|
July 1, 1973
Hemoglobin Abraham Lincoln, beta32 (B14) leucine leads to proline. An unstable variant producing severe hemolytic disease
G R Honig, D Green, M Shamsuddin, et al.
Blood
|
January 1, 1980
Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia
G R Honig, M Shamsuddin, R G Mason, et al.
Page
of 8