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Journal Articles

Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1

H Cave, B Gerard, E Martin, C Guidal, I Devaux, J Weissenbach, J Elion, E Vilmer, B Grandchamp

Blood (1995) 86 (10): 3869–3875.

https://doi.org/10.1182/blood.V86.10.3869.bloodjournal86103869

Published: 1995

Journal Articles

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site

N Parquet, I Devaux, L Boulanger, C Galand, P Boivin, MC Lecomte, D Dhermy, M Garbarz

Blood (1994) 84 (1): 303–308.

https://doi.org/10.1182/blood.V84.1.303.303

Published: 1994

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