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Journal Articles

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

S Hayette, D Dhermy, ME dos Santos, M Bozon, D Drenckhahn, N Alloisio, P Texier, J Delaunay, L Morle

Blood (1995) 85 (1): 250–256.

https://doi.org/10.1182/blood.V85.1.250.bloodjournal851250

Published: 1995

Journal Articles

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

S Feddal, S Hayette, F Baklouti, R Rimokh, R Wilmotte, JP Magaud, J Maréchal, EJ Benz, Jr, R Girot, J Delaunay, L Morlé

Blood (1992) 80 (11): 2925–2930.

https://doi.org/10.1182/blood.V80.11.2925.2925

Published: 1992

Journal Articles

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self- association site

N Alloisio, R Wilmotte, L Morlé, F Baklouti, J Maréchal, MT Ducluzeau, L Denoroy, C Féo, BG Forget, R Kastally, J Delaunay

Blood (1992) 80 (3): 809–815.

https://doi.org/10.1182/blood.V80.3.809.809

Published: 1992

Journal Articles

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

F Baklouti, J Maréchal, R Wilmotte, N Alloisio, L Morlé, MT Ducluzeau, L Denoroy, A Mrad, MH Ben Aribia, R Kastally, J Delaunay

Blood (1992) 79 (9): 2464–2470.

https://doi.org/10.1182/blood.V79.9.2464.2464

Published: 1992

Journal Articles

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps

S Feddal, G Brunet, L Roda, S Chabanis, N Alloisio, L Morle, MT Ducluzeau, J Marechal, JM Robert, EJ Benz, Jr, J Delaunay, F Baklouti

Blood (1991) 78 (8): 2113–2119.

https://doi.org/10.1182/blood.V78.8.2113.2113

Published: 1991

Journal Articles

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution

B Pothier, N Alloisio, J Marechal, L Morle, MT Ducluzeau, C Caldani, N Philippe, J Delaunay

Blood (1990) 75 (10): 2061–2069.

https://doi.org/10.1182/blood.V75.10.2061.2061

Published: 1990

Journal Articles

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

L Morle, F Morle, AF Roux, J Godet, BG Forget, L Denoroy, M Garbarz, D Dhermy, R Kastally, J Delaunay

Blood (1989) 74 (2): 828–832.

https://doi.org/10.1182/blood.V74.2.828.828

Published: 1989

Journal Articles

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state

N Alloisio, L Morle, B Pothier, AF Roux, J Marechal, MT Ducluzeau, Z Benhadji- Zouaoui, J Delaunay

Blood (1988) 71 (4): 1039–1047.

https://doi.org/10.1182/blood.V71.4.1039.1039

Published: 1988

Journal Articles

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

L Morle, N Alloisio, MT Ducluzeau, B Pothier, R Blibech, R Kastally, J Delaunay

Blood (1988) 71 (2): 508–511.

https://doi.org/10.1182/blood.V71.2.508.508

Published: 1988

Journal Articles

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis

B Pothier, L Morle, N Alloisio, MT Ducluzeau, C Caldani, C Feo, M Garbarz, I Chaveroche, D Dhermy, MC Lecomte

Blood (1987) 69 (6): 1759–1765.

https://doi.org/10.1182/blood.V69.6.1759.1759

Published: 1987

Journal Articles

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

F Baklouti, E Dorleac, L Morle, P Laselve, D Peyramond, M Aubry, J Godet, J Delaunay

Blood (1986) 67 (4): 957–961.

https://doi.org/10.1182/blood.V67.4.957.957

Published: 1986

Journal Articles

The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1

L Morle, M Garbarz, N Alloisio, R Girot, I Chaveroche, P Boivin, J Delaunay

Blood (1985) 65 (6): 1511–1517.

https://doi.org/10.1182/blood.V65.6.1511.bloodjournal6561511

Published: 1985

Journal Articles

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]

N Alloisio, L Morle, E Dorleac, O Gentilhomme, D Bachir, D Guetarni, P Colonna, M Bost, Z Zouaoui, L Roda

Blood (1985) 65 (1): 46–51.

https://doi.org/10.1182/blood.V65.1.46.46

Published: 1985

NARROW

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self- association site

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1

The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]

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American Society of Hematology

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American Society of Hematology

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