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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

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Kappa Lambda Light Chain, Urine
See also: Kappa/Lambda Quant Free Light Chain Ratio, Blood, Blood

Kappa/Lambda Quant Free Light Chain Ratio, Blood
See also: Kappa Lambda Light Chain, Urine

Karyotyping
Cell Culture (Biochemical and Molecular Studies), Amniotic Fluid, Skin, Fetal Tissue, Diaphragm, Other Tissue
Chromosomal Analysis, Amniotic Fluid
Chromosomal Analysis, Bone Marrow (for acquired and constitutional abnormalities)
Chromosomal Analysis, Fetal Blood (Prenatal Diagnosis)
Chromosomal Analysis, Peripheral Blood for Hematological Disorders
Chromosomal Analysis, Peripheral Blood, Cord Blood
Chromosomal Analysis, Product of Conception (POC)
Chromosomal Analysis, Skin or Internal Tissue or Blood from Autopsy
Chromosomal Analysis, Skin, Other Tissue
Chromosomal Breakage Studies, Peripheral Blood
FMR1 Gene Analysis Characterization of Alleles with Interpretation, Whole Blood

Ketones (Semi-Quantitative)
See also: Basic Metabolic Panel W/Calcium (CHEM8), Plasma
Beta Hydroxybutyrate, Plasma
Blood Gases (Arterial), Whole Blood (syringe only)
Urinalysis, Urine

17-Ketosteroids
See also: Cortisol, Urinary Free (HPLC), Urine

KIT (AML) Targeted Gene Analysis Exons 8, 17 with Interpretation, Whole Blood, Bone Marrow
See also: KIT (GIST) Targeted Gene Analysis Exons 9, 11, 13, 17 with Interpretation, Tissue
KIT Mutation (D816V) For Mast Cell Disease, Whole Blood, Bone Marrow or Tissue

KIT (GIST) Targeted Gene Analysis Exons 9, 11, 13, 17 with Interpretation, Tissue
See also: KIT (AML) Targeted Gene Analysis Exons 8, 17 with Interpretation, Whole Blood, Bone Marrow
KIT Mutation (D816V) For Mast Cell Disease, Whole Blood, Bone Marrow or Tissue

KIT Mutation (D816V) For Mast Cell Disease, Whole Blood, Bone Marrow or Tissue

Kleihauer-Betke Stain For Fetal Hemoglobin
Fetal Erythrocyte Quantitation, Maternal Peripheral Blood

Known Family Mutation (Renal Genetic Test), Whole Blood

Known Mutation (Deafness Genetic Test), Whole Blood

KOH Prep (Fungal Stain, KOH with Calcofluor White), Skin Scrapings, Hair, Nail Clippings

KRAS Gene Analysis Variants in codons 12 and 13 and Exon 3 with Interpretation


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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