Test Menu

Our test menu provides important information about the tests and services we offer to health care professionals and their patients. Our menu of tests is divided into two distinct categories – reproductive/genetics testing and oncology/pathology testing.

Please use our test menu search mechanism (below) to find the information you need. You can use the keyword search or choose a test name from the dropdown menus to learn more about our expansive menu or a specific test.

Please note, we enhance our services frequently and encourage you to revisit our test menu to receive the latest information.

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		Select a test .... - - - - - - - - - Oncology/Pathology Tests - - - - - - - - - ABL Kinase Domain Mutation Analysis in CML Alliance RQ-PCR Analysis AML1/ETO by PCR – t(8;21) by RT-PCR B-Cell Gene Rearrangements by PCR BCL-2 by PCR BCR-ABL - t(9;22) by RT-PCR (Quantitative) Bone Marrow - Peripheral Blood Smear Interpretation Bone Marrow - Smear Interpretation Bone Marrow Morphology - Complete Studies Bone Marrow Morphology - Cytochemistry Breast Cancer - DNA Ploidy/S-Phase Analysis by Flow Cytometry Breast Cancer - Individual Markers by IHC Breast Cancer - Interactive Quantitative Cellular Analysis (i QCA) Breast Cancer - Profiles Chromosome Analysis - Blood Chromosome Analysis - Bone Marrow Chromosome Analysis - Solid Tumor CLL-MRD (Minimial Residual Disease) by Flow Cytometry Colorectal Cancer - DNA Ploidy/S-Phase Analysis by Flow Cytometry Colorectal Cancer - Individual Markers by IHC Colorectal Cancer - Microsatellite Instability by PCR Colorectal Cancer - Profiles DNA Ploidy Analysis by Image Analysis DNA Ploidy/S-Phase Analysis by Flow Cytometry Drug Resistance Assay (DRA™) EGFR Amplification by FISH in NSCLC EGFR Mutation Analysis in NSCLC FIP1L1-PDGFRa Analysis in Hypereosinophilic Syndrome (HES) Disorders FISH (Fluorescence In Situ Hybridization) Flow Cytometry - interactiveFLOW Flow Cytometry, Six-Color (Immunophenotyping) Hematopathology Consultation Services HER2 by FISH (PathVysion) IgVH Mutation Analysis in B-CLL Immunohistochemistry (IHC) Immunohistochemistry (IHC) - Complex Tumor Analysis Immunohistochemistry (IHC) - Individual Markers Infectious Agents by Immunohistochemistry Infectious Agents by In Situ Hybridation Inv(16) RT-PCR JAK2 Mutation Analysis in Myeloproliferative Disorders KRAS Mutation Analysis Micrometastases - Bone Marrow/Peripheral Blood/Stem Cell Micrometastases - Melanoma/Carcinoma in Lymph Node Molar Pregnancy Evaluation (p57 and DNA Ploidy/S-Phase) Morphology – Special Stains p53 Mutation Analysis in B-CLL Pathology Consultation Services Peripheral Blood Smear Interpretation PML/RARA – t(15;17) by RT-PCR T-Cell Gene Rearrangements by PCR UGT1A1 Molecular Assay Urovysion™ by FISH - - - - - - - - - Reproductive/Genetics Tests - - - - - - - - - Acetylcholinesterase (AChE) Testing AFP3® - Triple Marker Test AFP4® - Quadruple Marker Test Amniotic Fluid Alphafetoprotein (AFAFP) Testing Angelman Syndrome Protocol Angiotensin Converting Enzyme (ACE) Analysis Ashkenazi Jewish Carrier Testing Bloom Syndrome Mutation Analysis Canavan Disease Mutation Analysis CFTR Intron 8 Poly (T) Analysis Chitotriosidase Assay Cri-Du-Chat Microdeletion Analysis Cystic Fibrosis Expanded Mutation Analysis - CFplus™ Cystic Fibrosis Gene Sequencing Cytogenetics – Amniotic Fluid Chormosome Analysis Cytogenetics – Blood Chromosome Analysis Cytogenetics – Chorionic Villi Sampling Chromosome Analysis Cytogenetics – Chromosome Breakage Analysis (Blood) Cytogenetics – Products of Conception (POC) Chromosome Analysis DiGeorge/Velocardiofacial (22q11) Syndrome Microdeletion Analysis Fabry Disease Enzyme Analysis Fabry Disease Mutation Analysis by Sequencing Factor II (Prothrombin) G20210A Mutation Analysis Factor V Leiden Mutation Analysis Familial Dysautonomia Mutation Analysis Fanconi Anemia Group C Mutation Analysis FirstScreen™ - First Trimester Screening Fragile X Syndrome Mutation Analysis Gaucher Disease Enzyme Analysis Gaucher Disease Mutation Analysis Glycogen Storage Disease Type 1a Mutation Analysis InSight (Interphase FISH for Rapid Detection of X, Y, 13, 18, 21) IntegratedScreen™ - Integrated Screening Kallmann Syndrome Microdeletion Analysis Maple Syrup Urine Disease (MSUD) Mutation Analysis Maternal Cell Contamination Analysis Maternal Serum Alphafetoprotein (MSAFP) Screening Microdeletion Analyses Miller-Dieker Syndrome Microdeletion Analysis MTHFR (C677T) Mutation Analysis Mucolipidosis Type IV Mutation Analysis Niemann-Pick Disease Type A Mutation Analysis Pompe Disease Test Pompe Disease Mutation Analysis (GAA) by Sequencing Prader-Willi Protocol Preimplantation Genetic Diagnosis (PGD) - Aneuploidy Preimplantation Genetic Diagnosis (PGD) - Translocations Rh c/E Mutation Analysis Rh D Mutation Analysis SequentialScreen™ SerumIntegratedScreen™ - Integrated Screening Sickle Cell Anemia Mutation Analysis Smith-Magenis Syndrome Microdeletion Analysis Spinal Muscular Atrophy (SMA) Steroid Sulfatase Deficiency (X-linked Ichthyosis) Subtelomere Analysis Tay-Sachs Disease Mutation Analysis Tay-Sachs Enzyme Analysis (Hexosaminidase A) TRAP (Tartrate Resistant Acid Phosphatase) Williams Syndrome Microdeletion Analysis Wolf-Hirschhorn Syndrome Microdeletion Analysis Y Chromosome Microdeletion Analysis Zygosity Testing   Search only Reproductive/Genetics Tests Search only Oncology/Pathology Tests