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Current Research in Translational Medicine|October 22, 2023
Cytogenetics in the management of hematologic neoplasms with germline predisposition: guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH)Nathalie Gachard, Marina Lafage-Pochitaloff, Julie Quessada, et al.
Annales De Pathologie|August 12, 2003
[Neurectodermal differentiation of extraskeletal myxoid chondrosarcoma: a classical feature?]Marie-Paule Algros, Marie-Agnès Collonge-Rame, Isabelle Bedgejian, et al.
European Journal of Haematology|December 16, 2011
Systematic donor blood qualification by flow cytometry would have been able to avoid CLL-type MBL transmission after unrelated hematopoietic stem cell transplantationChristophe Ferrand, Francine Garnache-Ottou, Marie Agnès Collonge-Rame, et al.
Oncology Reports|February 11, 2017
First description of a double heterozygosity for BRCA1 and BRCA2 pathogenic variants in a French metastatic breast cancer patient: A case reportGuillaume Meynard, Laura Mansi, Pierre Lebahar, et al.
Cancer Genetics and Cytogenetics|November 7, 2002
Identical abnormality of the short arm of chromosome 18 in two Philadelphia-positive chronic myelocytic leukemia patients with erythroblastic transformation, resulting in duplication of BCR-ABL1 fusionFlorence Nguyen Khac, Marie Christine Waill, Serge P Romana, et al.
Cancers|March 14, 2026
Germline BRCA1/2 Mutations in a Large Clinic-Based Cohort of Patients with Metastatic Breast Cancer in FranceGuillaume Meynard, Victor Pereira, Sophie Paget-Bailly, et al.
Genes, Chromosomes & Cancer|September 27, 2012
Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangementViolaine Havelange, Geneviève Ameye, Ivan Théate, et al.
Oncotarget|February 7, 2023
The "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility allelesMartin Chevarin, Diana Alcantara, Juliette Albuisson, et al.
Prenatal Diagnosis|March 29, 2016
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyNicolas Gruchy, Eleonore Blondeel, Nathalie Le Meur, et al.
Cancer Genetics and Cytogenetics|April 18, 2006
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique HématologiqueEric Jeandidier, Nicole Dastugue, Francine Mugneret, et al.
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