scholarly article | Q13442814 |
P50 | author | E Jennifer Edelman | Q86191217 |
P2093 | author name string | Patrick G Gallagher | |
Jon S Morrow | |||
Bernard G Forget | |||
Jose Sangerman | |||
Yelena Maksimova | |||
P2860 | cites work | Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy | Q28298978 |
Erythropoiesis: Hereditary Spherocytosis in Greece: Collective Data on a Large Number of Patients | Q30654000 | ||
Initiation of protein synthesis in mammalian cells with codons other than AUG and amino acids other than methionine | Q33777524 | ||
Abnormalities of erythrocyte membrane proteins in Korean patients with hereditary spherocytosis | Q34656872 | ||
Multigene amplification and massively parallel sequencing for cancer mutation discovery | Q35799619 | ||
P433 | issue | 10 | |
P921 | main subject | hereditary spherocytosis | Q541244 |
P304 | page(s) | 789-794 | |
P577 | publication date | 2008-10-01 | |
P1433 | published in | American Journal of Hematology | Q4744246 |
P1476 | title | Ankyrin-linked hereditary spherocytosis in an African-American kindred | |
P478 | volume | 83 |
Q26864442 | A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates |
Q38650691 | Ankyrin-1 Gene Exhibits Allelic Heterogeneity in Conferring Protection Against Malaria. |
Q53007604 | Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants. |
Q38718088 | Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis |
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