Search research articles
Contact Us
Filters
Showing results (21-30 of 94) with videos related to
Page
of 10
Sort By:
Blood Cells, Molecules & Diseases
|
January 1, 1996
Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis
P G Gallagher, B G Forget
The Journal of Biological Chemistry
|
November 3, 1995
Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis
P G Gallagher, B G Forget
Current Opinion in Hematology
|
March 1, 1997
Molecular basis of erythrocyte membrane disorders
P G Gallagher, J D Ferriera
Blood Cells, Molecules & Diseases
|
January 15, 1999
Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis
P G Gallagher, B G Forget
Pediatric Radiology
|
January 1, 1991
Cerebral infarctions due to CNS infection with Enterobacter sakazakii
P G Gallagher, W S Ball
The Journal of Biological Chemistry
|
January 27, 1998
An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene
P G Gallagher, B G Forget
Journal of Pediatric Gastroenterology and Nutrition
|
November 20, 1998
Understanding iron absorption and metabolism
P G Gallagher, R A Ehrenkranz
Blood
|
September 1, 1994
Spectrin St Louis and the alpha LELY allele
P G Gallagher, B G Forget
Pediatric Emergency Care
|
December 1, 1991
An approach to the diagnosis and treatment of membranous laryngotracheobronchitis in infants and children
P G Gallagher, C M Myer
Seminars in Hematology
|
January 1, 1993
Spectrin genes in health and disease
P G Gallagher, B G Forget
Page
of 10
Search research articles
Search
Showing results (21-30 of 94) with videos related to
Sort By:
Page
of 10
Blood Cells, Molecules & Diseases
|
January 1, 1996
Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis
P G Gallagher, B G Forget
The Journal of Biological Chemistry
|
November 3, 1995
Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis
P G Gallagher, B G Forget
Current Opinion in Hematology
|
March 1, 1997
Molecular basis of erythrocyte membrane disorders
P G Gallagher, J D Ferriera
Blood Cells, Molecules & Diseases
|
January 15, 1999
Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis
P G Gallagher, B G Forget
Pediatric Radiology
|
January 1, 1991
Cerebral infarctions due to CNS infection with Enterobacter sakazakii
P G Gallagher, W S Ball
The Journal of Biological Chemistry
|
January 27, 1998
An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene
P G Gallagher, B G Forget
Journal of Pediatric Gastroenterology and Nutrition
|
November 20, 1998
Understanding iron absorption and metabolism
P G Gallagher, R A Ehrenkranz
Blood
|
September 1, 1994
Spectrin St Louis and the alpha LELY allele
P G Gallagher, B G Forget
Pediatric Emergency Care
|
December 1, 1991
An approach to the diagnosis and treatment of membranous laryngotracheobronchitis in infants and children
P G Gallagher, C M Myer
Seminars in Hematology
|
January 1, 1993
Spectrin genes in health and disease
P G Gallagher, B G Forget
Page
of 10