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Every effort is being made to keep this directory comprehensive and up-to-date with respect to tests offered. However, should you not find what you are looking for, please email The Pathology Webmaster.

Laboratory tests arranged alphabetically

A B C D E F G H I J K L M N O P Q R S T U V W Y Z


Macroprolactin Check, Plasma

MAG Antibody Titer IgM by IFA
See also: MAG Antibody, IgM, Serum

MAG Antibody, IgM, Serum

MAG Antibody, IgM by Western Blot
See also: MAG Antibody, IgM, Serum

Magnesium, Plasma
See also: Magnesium-Other, Body Fluid

Magnesium, Urine 24 hr

Magnesium, Urine, Random

Magnesium-Other, Body Fluid
See also: Magnesium, Plasma

MAI Complex
Mycobacterial Culture

Malaria/Filaria
Blood Parasite Exam (R/O Malaria/Bld Parasites), Blood

Mandibuloacral Dysplasia with Typa A Lipodystrophy, MADA
Lamin (LMNA) Full Gene Sequence with Interpretation, Whole Blood

Manganese, Whole Blood

Mannose Binding Lectin, Serum

Marfan Syndrome
FBN1 Gene Analysis Full Gene Sequence, Whole Blood

Marijuana
THC (Marijuana) Confirmation, Random Urine

Mau
Microalbumin, Urine, Random

MDMA
Amphetamines, Urine Confirmation, Random Urine

Measles Antibody, IgG, Plasma

Measles IgM Antibody, Serum

MECP2 Gene Analysis Dup/Delet Variant, Whole Blood

MECP2 Gene Analysis Full Sequence, Whole Blood

MECP2 Sequencing
MECP2 Gene Analysis Full Sequence, Whole Blood

Medical/Legal Specimens

Melanoma Mutation Profiling, Formalin Fixed, Paraffin Embedded Tissue Block

MEN1 Gene Analysis Full Gene Sequence, Whole Blood

MEN2A
RET Full Gene Analysis, Whole Blood

MEN2B
RET Full Gene Analysis, Whole Blood

Meningitis/Encephalitis Panel, CSF, Lumbar puncture

Mercury, Random Urine

Mercury, Urine

Mercury, Whole Blood

Merosin-Deficient Congenital Muscular Dystrophy, Muscle or Skin Biopsy

Metanephrines Total, 24 hr Urine
See also: Catecholamines, Fractionated, 24 hr Urine
Homovanillic Acid, 24 hr Urine
Vanillylmandelic Acid, 24 hr Urine

Metanephrines Total, Random Urine
See also: Catecholamines, Fractionated, Random Urine
Homovanillic Acid, Random Urine
Vanillylmandelic Acid, Random Urine

Metanephrines, Free, Plasma

Methadone & Metabolite, Random Urine

Methadone Drug Level, Serum

Methamphetamine
Amphetamines, Urine Confirmation, Random Urine

Methanol
Alcohols Panel (Methanol, Ethanol, Isopropanol, Acetone), Plasma
Ethanol/Volatiles Screen (EVS), Plasma

Methemoglobin, Whole Blood

Methicillin Resistant Staphylococcus aureus
Staphylococcus aureus (MRSA/MSSA) by PCR, Surveillance Swab Specimen collected from Nares

Methionine
Amino Acids, Quantitative, Plasma
Amino Acids, Quantitative, Random Urine

Methotrexate Drug Level, Plasma

3-Methylglutaconic Acid, Blood

3-Methylglutaconic Acid, Urine

Methylmalonic Acid, Blood

Methylmalonic Acid, Urine (24 hr or random)

5-Methyltetrahydrofolate, CSF

Metoprolol (Lopressor) Drug Level, Serum or Plasma

MGMT Methylation Detection by PCR, Tumor Tissue

MIC
Antimicrobial Susceptibility Profile MIC, (Per Organism)

MICA Genotyping Intermediate Resolution (VAMC), Whole Blood

Microalbumin, Urine, Random

Microalbumin, Timed Collection, Urine

Microarray-Constitutional, Whole Blood from lavender top (EDTA) tube; Fetal Tissue, Other Tissue

Microbiology Specimen Collection Procedures
See information in appendix:
Microbiology Specimen Collection and Transport

Microsatellite Instability PCR with Interpretation

Microsomal Antibody
Thyroid Peroxidase Antibody, Plasma

Miscellaneous Test, Urine

Miscellaneous Test, Whole Blood/Serum/Plasma

Miscellaneous Test - Other, Test dependent

Miscellaneous Test, Genetic, Test dependent

Mismatch Repair Protein Immunohistochemistry, Formalin Fixed, Paraffin Embedded Tissue containing Tumor

Mito/Met ACGH DNA Analysis, Whole Blood

Mitochondrial M2 Ab, IgG, Serum

Mitotane Level, Plasma

Mix PTT Panel, Plasma

Miyoshi Myopathy
Dysferlin (DYSF) Full Gene Sequence with Interpretation, Whole Blood

MLH1 Promoter Methylation, Paraffin, Tumor Tissue

Mo-1 Deficiency
Leukocyte Adhesion Deficiency Panel, Whole Blood

Molecular Cytogenetics
Fluorescence In-Situ Hybridization (FISH-Aneuploidy Screening), Peripheral Blood (Newborn or Cord, and Others)
Fluorescence In-Situ Hybridization (FISH-Bladder Carcinoma), Voided Urine, Bladder Wash
Fluorescence In-Situ Hybridization (FISH-Bone Marrow), Bone Marrow, Hematologic Malignancies, Lymph Node, Fine-Needle Aspirate, Pleural Effusion, CSF
Fluorescence In-Situ Hybridization (FISH-Hematological Blood), Peripheral Blood
Fluorescence In-Situ Hybridization (FISH-Microdeletion), Peripheral Blood, Fibroblasts, Other Tissue
Fluorescence In-Situ Hybridization (FISH-Prenatal-Aneuploidy/Microdeletion), Amniocytes, Chorionic Villi
Fluorescence In-Situ Hybridization (FISH-Tumors), Tumor Tissue

Molybdenum, Plasma

Mononucleosis Test
Heterophile Antibody (Monospot) IRL Only, Plasma

Monospot Test
Heterophile Antibody (Monospot) IRL Only, Plasma

MORL ADAMTS-13 Activity, Plasma

MORL ADAMTS-13 Inhibitor Only, Plasma

MORL ADAMTS-13 with Reflex to Inhibitor, Plasma
See also: MORL ADAMTS-13 Activity, Plasma
MORL ADAMTS-13 Inhibitor Only, Plasma

MORL Soluble MAC, Whole Blood

Morphine
Opiate, Confirmation, Random Urine

Mould Culture
Fungal Culture

MPL codon 515 Mutation, Blood

MPL codon 515 Mutation, Bone Marrow Aspirate

MS Screen
Multiple Sclerosis Screen Panel, Serum & CSF

MT-RNR1 Gene Analysis Common Variants, Whole Blood

MT-TL1 Gene Analysis Common Variants, Whole Blood

MT-TS1 Gene Analysis Common Variants, Whole Blood

MTB Culture
Mycobacterial Culture

MTHFR Mutation Analysis with Interpretation, Whole Blood

Mucopolysaccharides, Quantitation, Random Urine

Multiple Sclerosis Screen Panel, Serum & CSF

Mumps IgG Antibody Detection, Plasma

Mumps IgM Antibody, Serum

Mumps PCR, Buccal Swab

Muscle Biopsy, Fresh or Frozen Tissue

Muscle-Eye-Brain Disease
POMGNT1 Full Gene Sequence with Interpretation, Whole Blood

Muscular Dystrophy Testing, Tissue or Blood
Congenital Muscular Dystrophy, Muscle or Skin Biopsy
DMD Gene Analysis Dup/Delet Variants, Whole Blood
Duchenne/Becker Muscular Dystrophy, Muscle Biopsy
Emery-Dreifuss Muscular Dystrophy, Muscle or Skin Biopsy
FSHD - Detection of Abnormal Alleles with Interpretation (FSHD1 and FSHD2), Whole Blood - 15 mL in EDTA tubes
Limb Girdle Muscular Dystrophy (LGMD), Muscle Biopsy
Merosin-Deficient Congenital Muscular Dystrophy, Muscle or Skin Biopsy
Sarcoglycan-Deficient Limb Girdle Muscular Dystrophy, Muscle Biopsy

Muscular Dystrophy, MDA
DMD Gene Analysis Dup/Delet Variants, Whole Blood

MuSK Antibody Test, Serum

Myasthenia gravis
Acetylcholine Receptor Binding Antibody, Serum
Neurology Myasthenia Gravis Reflexive Panel, Serum

Mycobacteria Tuberculosis PCR with Rifampin Resistance (includes culture and stain), Sputum, Induced Sputum, Bronchoalveolar Lavage or Bronchial Washings

Mycobacterial Culture
See also: Bacterial Culture

Mycology Culture
Fungal Culture

Mycophenolic Acid Drug Level, Serum

Mycoplasma Antibody, IgG + IgM, Serum

Mycoplasma PCR, Throat Swab

Mycoplasma pneumoniae Antibody, IgG , Serum
See also: Mycoplasma pneumoniae Antibody, IgM, Serum

Mycoplasma pneumoniae Antibody, IgM, Serum
See also: Mycoplasma pneumoniae Antibody, IgG , Serum

Mycoplasma pneumoniae by PCR, Respiratory Specimen

MYD88 Exon 5 Sequencing, FFPE Tissue, Peripheral Blood, Bone Marrow Aspirate

Myelin Basic Protein, CSF

Myeloperoxidase Antibodies, IgG, Serum

Myoglobin, Plasma

Myoglobin, Urine (random)

Myositis Specific Antibody Profile, Serum

Mysoline
Primidone And Metabolite Drug Level, Plasma


A B C D E F G H I J K L M N O P Q R S T U V W Y Z


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