Laboratory Medicine


Detection of cytogenetic and molecular abnormalities in leukemias, lymphomas and solid tumors by standard and molecular cytogenetics and molecular pathology

  1. Prenatal/postnatal diagnosis of microdeletion syndromes and numerical aberrations
  2. Array comparative genomic hybridization for detection of copy number variants
  3. 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
  • 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

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