| scholarly article | Q13442814 |
| P2093 | author name string | Y. Yawata | |
| C. Galand | |||
| J. Delaunay | |||
| D. Dhermy | |||
| M. Garbarz | |||
| A. Kanzaki | |||
| T. K. Tang | |||
| J. Maréchal | |||
| R. Wilmotte | |||
| P2860 | cites work | Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 |
| Growth of Plasmodium falciparum in human erythrocytes containing abnormal membrane proteins | Q33808075 | ||
| Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46. | Q33899236 | ||
| Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans | Q34265298 | ||
| Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis | Q35815997 | ||
| Sp alpha I/65 hereditary elliptocytosis in North Africa | Q38870067 | ||
| Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African origin | Q38968871 | ||
| Dried blood spot on filter paper as a source of mRNA | Q40422037 | ||
| Three RFLPs are detected by an alpha spectrin genomic clone | Q40567257 | ||
| Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele | Q41208228 | ||
| Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening | Q69580527 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | gene frequency | Q71131180 |
| P304 | page(s) | 553-556 | |
| P577 | publication date | 1995-07-01 | |
| P1433 | published in | British Journal of Haematology | Q4970200 |
| P1476 | title | Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-gene | |
| Ethnic distribution of allele aLELY, a low‐expression allele of red‐cell spectrin a‐gene | |||
| P478 | volume | 90 |
| Q50237691 | Clinical utility of next-generation sequencing in the diagnosis of hereditary haemolytic anaemias |
| Q41634665 | Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis |
| Q49927544 | KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity |
| Q37377942 | Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defects |
| Q47768550 | Presence of allele alphaLELY in an Amazonian Indian population |
| Q92105504 | The Spectrum of SPTA1-Associated Hereditary Spherocytosis |
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