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Journal Articles

Neonatal Hemolytic Anemia Due to Inherited Harderoporphyria: Clinical Characteristics and Molecular Basis

J. Lamoril, H. Puy, L. Gouya, R. Rosipal, V. Da Silva, B. Grandchamp, T. Foint, B. Bader-Meunier, J.P. Dommergues, J.C. Deybach, Y. Nordmann

Blood (1998) 91 (4): 1453–1457.

https://doi.org/10.1182/blood.V91.4.1453

Published: 1998

Journal Articles

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

S Raynaud, H Cave, M Baens, C Bastard, V Cacheux, J Grosgeorge, C Guidal-Giroux, C Guo, E Vilmer, P Marynen, B Grandchamp

Blood (1996) 87 (7): 2891–2899.

https://doi.org/10.1182/blood.V87.7.2891.bloodjournal8772891

Published: 1996

Journal Articles

Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distribution

V Picard, F Renaudie, C Porcher, MW Hentze, B Grandchamp, C Beaumont

Blood (1996) 87 (5): 2057–2064.

https://doi.org/10.1182/blood.V87.5.2057.2057

Published: 1996

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

Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Gunther's disease)

JC Deybach, H de Verneuil, S Boulechfar, B Grandchamp, Y Nordmann

Blood (1990) 75 (9): 1763–1765.

https://doi.org/10.1182/blood.V75.9.1763.1763

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

NARROW

Neonatal Hemolytic Anemia Due to Inherited Harderoporphyria: Clinical Characteristics and Molecular Basis

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distribution

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

Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Gunther's disease)

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

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ASH Publications

American Society of Hematology

Neonatal Hemolytic Anemia Due to Inherited Harderoporphyria: Clinical Characteristics and Molecular Basis

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

Overexpression of the ferritin H subunit in cultured erythroid cells changes the intracellular iron distribution

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

Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Gunther's disease)

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

Email alerts

ASH Publications

American Society of Hematology

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