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Blood
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November 11, 1975
Hereditary stomatocytosis: membrane and metabolism studies
W C Mentzer, W B Smith, J Goldstone, et al.
Blood
|
February 1, 1980
G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia
W C Mentzer, R Warner, J Addiego, et al.
The Journal of Pediatrics
|
October 1, 1976
Developmental change in red blood cell volume: implication in screening infants and children for iron deficiency and thalassemia trait
M A Koerper, W C Mentzer, G Brecher, et al.
Biochimica Et Biophysica Acta
|
June 24, 1982
Modification of hemoglobin S with dimethyl adipimidate. Contribution of individual reacted subunits to changes in properties
R Pennathur-Das, R H Heath, W C Mentzer, et al.
The American Journal of Pediatric Hematology/Oncology
|
February 1, 1994
Availability of related donors for bone marrow transplantation in sickle cell anemia
W C Mentzer, S Heller, P R Pearle, et al.
Biochimica Et Biophysica Acta
|
November 21, 1984
Two-dimensional electrophoretic analysis of human erythrocyte cylindrin
W M Lande, P V Thiemann, K A Fisher, et al.
American Journal of Medical Genetics
|
April 1, 1984
Prenatal diagnosis of chronic granulomatous disease
K K Matthay, M S Golbus, D W Wara, et al.
California Medicine
|
October 1, 1973
Letter: Sickle cell trait in the sky
C F Catlett, W B Smith, W C Mentzer, et al.
British Journal of Haematology
|
July 1, 1977
An unusual form of chronic neutropenia in a father and daughter with hypogammaglobulinaemia
W C Mentzer, R B Johnston, R L Baehner, et al.
The Journal of Pediatrics
|
February 1, 1976
Iron deficiency in an Eskimo village. The value of serum ferritin in assessing iron nutrition before and after a three-month period of iron supplementation
J M Burks, M A Siimes, W C Mentzer, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 100) with videos related to
Sort By:
Page
of 10
Blood
|
November 11, 1975
Hereditary stomatocytosis: membrane and metabolism studies
W C Mentzer, W B Smith, J Goldstone, et al.
Blood
|
February 1, 1980
G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia
W C Mentzer, R Warner, J Addiego, et al.
The Journal of Pediatrics
|
October 1, 1976
Developmental change in red blood cell volume: implication in screening infants and children for iron deficiency and thalassemia trait
M A Koerper, W C Mentzer, G Brecher, et al.
Biochimica Et Biophysica Acta
|
June 24, 1982
Modification of hemoglobin S with dimethyl adipimidate. Contribution of individual reacted subunits to changes in properties
R Pennathur-Das, R H Heath, W C Mentzer, et al.
The American Journal of Pediatric Hematology/Oncology
|
February 1, 1994
Availability of related donors for bone marrow transplantation in sickle cell anemia
W C Mentzer, S Heller, P R Pearle, et al.
Biochimica Et Biophysica Acta
|
November 21, 1984
Two-dimensional electrophoretic analysis of human erythrocyte cylindrin
W M Lande, P V Thiemann, K A Fisher, et al.
American Journal of Medical Genetics
|
April 1, 1984
Prenatal diagnosis of chronic granulomatous disease
K K Matthay, M S Golbus, D W Wara, et al.
California Medicine
|
October 1, 1973
Letter: Sickle cell trait in the sky
C F Catlett, W B Smith, W C Mentzer, et al.
British Journal of Haematology
|
July 1, 1977
An unusual form of chronic neutropenia in a father and daughter with hypogammaglobulinaemia
W C Mentzer, R B Johnston, R L Baehner, et al.
The Journal of Pediatrics
|
February 1, 1976
Iron deficiency in an Eskimo village. The value of serum ferritin in assessing iron nutrition before and after a three-month period of iron supplementation
J M Burks, M A Siimes, W C Mentzer, et al.
Page
of 10