Detection of cytogenetic and molecular abnormalities in leukemias, lymphomas and solid tumors by standard and molecular cytogenetics and molecular pathology
- Prenatal/postnatal diagnosis of microdeletion syndromes and numerical aberrations
- Array comparative genomic hybridization for detection of copy number variants
- Routine (high volume) testing<
- Bone marrow and peripheral smear examination
- Cytogenetics
- Flow cytometry
- Hemoglobinopathy
- Lymphoma consultation
- Molecular testing
- Routine hematology
- Routine and specialized coagulation.
- Specialized disease/organ system-related testing
- Toxicology and therapeutic drug monitoring, electrophoresis
- Protein electrophoesis
- Hemoglobinopathy screening
- Clinical Diagnostics
- Immunohistochemistry
- CTC Veridex Cellsearch Circulating Tumor Cell Detection
- Molecular Assays
- Anaerobes
- Antimicrobials
- Bacteriology
- Molecular Microbiology
- Mycobacteriology
- Mycology
- Parasitology
- Serology
- Virology
- CTC
- Ki67
- MGMT
- PTEN
- EGRFvIII RT PCR
- UroVysion FISH
- B-Cell Gene Rearrangement
- bcl-2 Gene Rearrangement
- bcr/abl Gene Rearrangement
- Bone Marrow Transplant Engraftment
- BRAF Gene Mutation Detection
- BRCA Ashkenazi Jewish Mutations
- c-kit Mutation Detection for Systemic Mastocytosis
- Cystic Fibrosis Mutation Analysis
- DNA Fingerprinting
- Factor V Mutation Analysis
- Familial Mediterranean Fever Mutation
- Fragile X Mutation Analysis
- Friedreich's Ataxia Mutation Analysis
- Hereditary Hemochromatosis
- Huntington Disease
- JAK2 Mutation Analysis
- KRAS Gene Mutation Detection
- Microsatellite Instability
- MTHFR Variants Detection
- Paternity Testing
- PML/RAR Alpha t(15;17) Translocation
- Postnatal Chromosomal Microarray
- Prothrombin 20210A Variant
- Sex Identity
- T-Cell Gene Rearrangement
- Twin Zygosity
- Custom Mutation Analysis (please contact us to discuss)
- Cystic Fibrosis, Full Gene Sequencing
- Familial Mediterranean Fever, Full Gene Sequencing
- Hereditary Inclusion Body Myopathy M712T Mutation Analysis
- IDH1 Mutation Detection
- IDH2 Mutation Detection
- Nijmegen Breakage Syndrome, Full Gene Sequencing
- Nijmegen Breakage Syndrome, 657del5 Mutation Analysis
- PTEN, Full Gene Sequencing
- Her-2/neu by FISH
- Grossing specimens
- Sentinel lymph node protocol
- Diagnostic comprehensive interpretations
- Consultation for challenging breast cancer cases
- Molecular assessment of breast cancers
- Clinical genomic assessment of breas cancer risk
- Breast biomarkers by IHC stains (ER, PR, Her-2/neu, and Ki-67)
- Review of surgical pathology specimens (i.e., heart and lung biopsies, excised native and artificial heart valves and blood vessels
- Consultation services on complex autopsy specimens (complex congenital heart diseases; hearts with implanted mechanical evices such as ventricle
- assist devices, artificial valves and arterial stents).
- Fine needle aspirations
- Adjunct tests for urine cytology including UroVysion and ImmunoCyt
- Tissue consultation
- Direct immunofluorescence studies
- Comprehensive immunohistochemistry staining
- Immunohistochemistry
- Molecular studies for GI malignancies including carcinoma, lymphoma and sarcoma
- Rapid diagnosis of biopsy specimens
- Electron microscopy
- Flourescence microscopy
