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Publications by G Tchernia

An Isoform-Specific Mutation in the Protein 4.1 Gene Results in Hereditary Elliptocytosis and Complete Deficiency of Protein 4.1 in Erythrocytes but Not in Nonerythroid Cells.

Journal of Clinical Investigation
Medicine
1993English

Deficiency of Skeletal Membrane Protein Band 4.1 in Homozygous Hereditary Elliptocytosis. Implications for Erythrocyte Membrane Stability.

Journal of Clinical Investigation
Medicine
1981English

Effectiveness of Partial Splenectomy in Red Cell Membrane Defects, a Twelve Year Experience 26

Pediatric Research
Child HealthPediatricsPerinatology
1997English

ESPHI DBA Working Group: PERSPECTIVES AND FUTURE COLLABORATION

Pediatric Research
Child HealthPediatricsPerinatology
1999English

Recombinant Erythropoietin in Infants With Hereditary Spherocytosis

Pediatric Research
Child HealthPediatricsPerinatology
1999English

Nouveaux Indices Sur La Relation Ribosome - Hématopoïèse ?

Medecine/Sciences
BiochemistryMedicineGeneticsMolecular Biology
1999English

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