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Journal Articles

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

M Garbarz, MC Lecomte, C Feo, I Devaux, C Picat, C Lefebvre, F Galibert, H Gautero, O Bournier, C Galand

Blood (1990) 75 (8): 1691–1698.

https://doi.org/10.1182/blood.V75.8.1691.1691

Published: 1990

Journal Articles

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

MC Lecomte, M Garbarz, B Grandchamp, C Feo, H Gautero, I Devaux, O Bournier, C Galand, L d'Auriol, F Galibert

Blood (1989) 74 (3): 1126–1133.

https://doi.org/10.1182/blood.V74.3.1126.1126

Published: 1989

Journal Articles

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

M Garbarz, MC Lecomte, D Dhermy, C Feo, I Chaveroche, H Gautero, O Bournier, C Picat, A Goepp, P Boivin

Blood (1986) 67 (6): 1661–1667.

https://doi.org/10.1182/blood.V67.6.1661.1661

Published: 1986

Journal Articles

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

MC Lecomte, D Dhermy, C Solis, A Ester, C Feo, H Gautero, O Bournier, P Boivin

Blood (1985) 65 (5): 1208–1217.

https://doi.org/10.1182/blood.V65.5.1208.1208

Published: 1985

Journal Articles

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis

M Garbarz, D Dhermy, MC Lecomte, C Feo, I Chaveroche, C Galand, O Bournier, O Bertrand, P Boivin

Blood (1984) 64 (5): 1006–1015.

https://doi.org/10.1182/blood.V64.5.1006.1006

Published: 1984

NARROW

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis

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ASH Publications

American Society of Hematology

Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosis

Email alerts

ASH Publications

American Society of Hematology

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