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Hemoglobin|January 1, 1988
Hemoglobin Pierre-Bénite [beta 90(F6)Glu----Asp], a new high affinity variant found in a French familyF Baklouti, Y Giraud, A Francina, et al.
Scandinavian Journal of Haematology|September 1, 1984
The Hb F composition in a Moroccan family with beta zero-thalassaemia and Hb O-ArabF Morlé, L Morlé, F Baklouti, et al.
American Journal of Hematology|December 1, 1982
Kinetic alterations of the red cell membrane phosphatase in alpha- and beta-thalassemiaL Morlé, E Dorléac, N Alloisio, et al.
American Journal of Hematology|April 1, 1996
Hemoglobin Debrousse (beta 96[FG3]Leu-->Pro): a new unstable hemoglobin with twofold increased oxygen affinityP Lacan, J Kister, A Francina, et al.
American Journal of Hematology|November 1, 1987
Association in cis of beta +-thalassemia and hemoglobin SF Baklouti, A Francina, E Dorléac, et al.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
Hemoglobin|January 1, 1984
The association of hemoglobin Knossos and hemoglobin Lepore in an Algerian patientL Morlé, F Morlé, E Dorléac, et al.
British Journal of Haematology|January 1, 1989
Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosisL Morlé, B Pothier, N Alloisio, et al.
Biomedica Biochimica Acta|January 1, 1983
The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosisN Alloisio, E Dorleac, L Morle, et al.
Haematologica|May 9, 1998
Hereditary spherocytosis: from clinical to molecular defectsA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
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