Disease: Congenital chromosomal disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 Biomarker group BEFREE Association of cytogenetic abnormalities with detection of BCR-ABL fusion transcripts in children with T-lineage lymphoproliferative diseases (T-ALL and T-NHL). 14752867 2004
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 Biomarker group BEFREE To test the feasibility of the FISH strategies, 30 samples from patients with B-NHL with cytogenetic abnormalities of 3q27 were evaluated with both assays. 11516111 2001
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.030 GeneticVariation group BEFREE The clinical features, morphology and immunophenotype of 20 cases of B non Hodgkin's lymphoma (B-NHL) with chromosome abnormalities involving 11q13-14 were studied, to determine if this abnormality was closely associated with a specific sub-type of B-NHL. 1643018 1992