Cases (2) Phenotype (2) Patients (2) Cases (2) Patients (2) recherche (1) association (1) mutation (1) perte (1) analyse (1) gène (1) maladie (1) point (1) Diagnosis (1) Deletion (1) Defects (1) Cytogenetics (1) Counseling of (1) Causative (1) Case (1) Description and travel (1) Workflow (1) Molecular diagnosis (1) Genes (1) Acute myeloid leukemia (1) In situ hybridization (1) Acute leukemia (1) Tumors (1) Transcription (1) Social groups (1)