C. Guidal

发表

Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm

H. Cavé, B. Gérard, B. Grandchamp, 1997, Leukemia.

Analysis of the 5′ flanking sequence of the Gγ globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu βs haplotype

J. Elion, G. Tachdjian, C. Sayada, 1992, Human Genetics.

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.

J. Weissenbach, H. Cavé, B. Gérard, 1995, Blood.

Compound heterozygosity for ΔF508 and F508C: A cautionary note on the molecular diagnosis of cystic fibrosis

E. Denamur, J. Oury, J. Elion, 1994 .

Is Very Common in Childhood Acute Lymphoblastic Leukemia and Permits the Precise Localization of a Tumor-Suppressor Gene Distinct From p7 KIP1

I. Devaux, E. Vilmer, C. Guidal, 2002 .

A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia.

H. Cavé, B. Grandchamp, J. Elion, 1996, Leukemia.

A competitive PCR-based method using TCRD, TCRG and IGH rearrangements for rapid detection of patients with high levels of minimal residual disease in acute lymphoblastic leukemia

H. Cavé, B. Grandchamp, E. Vilmer, 2002, Leukemia.

Potential antileukemic effect of gamma delta T cells in acute lymphoblastic leukemia.

P. Rohrlich, B. Grandchamp, L. Boumsell, 1995, Leukemia.

Prospective monitoring and quantitation of residual blasts in childhood acute lymphoblastic leukemia by polymerase chain reaction study of delta and gamma T-cell receptor genes.

H. Cavé, P. Rohrlich, O. Fenneteau, 1994, Blood.

Clinical Significance of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia

H. Cavé, B. Grandchamp, K. Thielemans, 1998 .

Four-color flow cytometry bypasses limitations of IG/TCR polymerase chain reaction for minimal residual disease detection in certain subsets of children with acute lymphoblastic leukemia.

H. Cavé, P. Rohrlich, F. Garnache-Ottou, 2005, Haematologica.

Expansion of polyclonal B-cell precursors in bone marrow from children treated for acute lymphoblastic leukemia.

H. Cavé, P. Rohrlich, O. Fenneteau, 1997, Hematology and cell therapy.

Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia. European Organization for Research and Treatment of Cancer--Childhood Leukemia Cooperative Group.

H. Cavé, B. Grandchamp, K. Thielemans, 1998, The New England journal of medicine.

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children.

J. Elion, M. Maier‐Redelsperger, R. Ducrocq, 1993, Blood.