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- Detection of cytogenetic abnormalities in leukemias, lymphomas and solid tumors by classic and molecular cytogenetics methods on fresh and archival tissue.
- Diagnosis of microdeletion syndromes and numerical aberrations in prenatal and postnatal cases.
- Identification of small genetic aberrations in individuals with congenital diseases using high resolution genomic microarray technologies.
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- Rapid fluorescence in situ hybridization (FISH) for Aneuploidy Screening
- Interphase analysis for trisomies of 13, 18 and 21, and aneuploidies of chromosomes X and Y provides rapid detection of the most common chromosomal aneuploidies
- Routine G-band Chromosome Analysis
- Performed to obtain an overview of the fetal karyotype and chromosome structure in amniocytes, chorionic villi sampling and products of conception
- SNP -Chromosomal Microarray Analysis (CMA) offers full genome coverage with nearly 2 million oligonucleotide markers
- Routine G-band Chromosome Analysis for couples with infertility or recurrent pregnancy loss
- Routine G-band Chromosome Analysis
- Comprehensive FISH panels
- Acute Lymphocytic Leukemia (T-B ALL)
- Acute Myelogenous Leukemia (AML),
- Myelodysplastic Syndrome (MDS)
- Myeloproliferative Neoplasms (MPN)
- Chronic Myelogenous Leukemia (CML)
- Non-Hodgkin’s Lymphoma (NHL)
- Plasma Cell Myeloma
- Chronic Lymphocytic Leukemia (CLL)
- Lymphoproliferative Disorder (LPD)
- Uveal melanoma
- Brain, CNS (Glioma, Neuroblastoma, Schwannoma/Rhabdoid)
- Bladder
- Breast
- Soft tissue Sarcoma (Ewing, Alveolar rhabdomyosarcoma, Myxoid/round cell liposarcoma, Malignant Liposarcoma/Angiomatoid fibrous histiocytoma, Well-differentiated liposarcoma)
Our extensive menu of FISH probes is available upon request and includes several commercially available for oncology, prenatal and postnatal testing. |
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No current publications |
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