Cytogenetics
Molecular Cytogenetics
- Array CGH - Comparative Genomic Hybridization
- Centromeric Multiprobe System
- Chromosome 6 aneuploidies detection by FISH
- Chromosome 9 aneuploidies detection by FISH
- Detection by FISH of 11q23 deletion
- Detection by FISH of 13q14.3 deletion
- Detection by FISH of 20q12 deletion
- Detection by FISH of 5q31 deletion
- Detection by FISH of 5q33-34 deletion
- Detection by FISH of 6q21 deletion
- Detection by FISH of 7q31 deletion
- Detection by FISH of 9q34 deletion
- Detection by FISH of ALK rearrangements [del(2p); t(2;5)]
- Detection by FISH of aneuploidies on uncultured amniotic fluid
- Detection by FISH of ATM (11q22.3) rearrangements
- Detection by FISH of BCL-6 (3q27) rearrangements
- Detection by FISH of CBFB rearrangements [(inv(16)/t(16;16)]
- Detection by FISH of chromosome 12 trisomy
- Detection by FISH of chromosome 8 trisomy
- Detection by FISH of c-MYC (8q24) rearrangements
- Detection by FISH of DiGeorge Syndrome
- Detection by FISH of IGH (14q23) rearrangements
- Detection by FISH of MALT1 (18q21) rearrangements
- Detection by FISH of Miller-Dieker Syndrome
- Detection by FISH of MLL (11q23) rearrangements
- Detection by FISH of p16 (9p21) deletion
- Detection by FISH of Phelan-McDermid Syndrome
- Detection by FISH of Prader-Willi/Angelman Syndrome
- Detection by FISH of PTEN (10q23) deletion
- Detection by FISH of RARa (17q21) rearrangements
- Detection by FISH of sexual chromosomes (X/Y)
- Detection by FISH of Smith-Magenis Syndrome
- Detection by FISH of subtelomeric rearrangements
- Detection by FISH of t(11;14) IGH/CCND1
- Detection by FISH of t(11;18) API2/MALT1
- Detection by FISH of t(12;21) ETV6/AML1
- Detection by FISH of t(14;16) IGH/MAF
- Detection by FISH of t(14;18) IGH/BCL2
- Detection by FISH of t(14;18) IGH/MALT1
- Detection by FISH of t(15;17) PML/RARA
- Detection by FISH of t(4;14) IGH/FGFR3
- Detection by FISH of t(8;14) MYC/IGH
- Detection by FISH of t(8;21) AML1/ETO1
- Detection by FISH of t(9;22) BCR/ABL
- Detection by FISH of TP53 (17p13.1) deletion/amplification
- Detection by FISH of Williams Syndrome
- Detection by FISH of Wolf-Hirschhorn Syndrome
- FISH analysis of sexual chromosomes (X/Y)
- FISH analysis with centromeric probe
- FISH analysis with painting probe
- FISH analysis with subtelomeric probe
- FISH analysis with unique sequence probe
- OncoFish for CLL (13q-, 11q-, 17p-, +12, IGH)
- OncoFish for MDS (5q-, 7q-, 20q-)
- OncoFish for MM [13q-, 17p-, t(4;14), t(11;14)]
Classic Cytogenetics
- Chromosome analysis of amniotic fluid
- Chromosome analysis of chorionic villi
- Chromosome analysis of non-stimulated cultures (bone marrow and/or peripheral blood)
- Chromosome analysis of stimulated cultures (fetal blood)
- Chromosome analysis of stimulated cultures (peripheral blood)
- Chromosome analysis of tissue fibroblasts
- Chromosome breakage analysis
- Fibroblasts cell culture (amniotic fluid/chorionic villi)
- Fibroblasts cell culture (tissue)
- Lymphocyte cell culture
- Lymphocyte culture (bone marrow)
