Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Chromosome 15 Uniparental Disomy Analysis (UPD15) Chromosome 15 Uniparental Disomy Analysis (UPD15)
Chromosome 15 UPD, Uniparental disomy (chromosome 15), UPD 15, Prader-Willi syndrome (chromosome 15 UPD), Angelman syndrome (chromosome 15 UPD)
Chromosome Analysis (High Resolution), Peripheral Blood Peripheral Blood, Chromosome Analysis
Blood chromosome analysis, Blood karyotyping, Peripheral blood chromosome analysis, Peripheral blood karyotype (high resolution)
Chromosome Analysis, Amniotic Fluid Amniotic Fluid Chromosome Analysis, Standard
Amniotic fluid karyotype, Amnioticentesis sample karyotype, Amniocyte karyotype, Amniotic fluid karyotyping, Prenatal chromosome analysis, NIPT / NIPS confirmation study
Chromosome Analysis, Percutaneous Umbilical Blood (PUBS) Percutaneous Umbilical Blood Chromosome Analysis
Chromosome Analysis, Percutaneous Umbilical Blood Sample (PUBS), Percutaneous Umbilical Blood Sample, Chromosome Analysis, Percutaneous umbilical blood sampling (PUBS), PUBS chromosome analysis, PUBS karyotype analysis, Karyotype on percutaneous umbilical blood sample, Fetal blood karyotype, PUBS karyotyping, Cordocentesis
Chromosome Analysis, Tissue (Postnatal, POC, or Autopsy) Tissue Chromosome Analysis
Tissue chromosome analysis, Tissue karyotype analysis, Skin biopsy chromosome analysis, Skin biopsy karyotype analysis, Fibroblast chromosome analysis, Fibroblast karyotype analysis, Autopsy chromosome analysis, Tissue karyotyping, Surgical tissue chromosome analysis, Autopsy tissue chromosome analysis, Products of conception (POC) chromosome analysis, POC chromosome analysis, Placental tissue chromosome analysis, Fetal tissue chromosome analysis, Umbilical cord tissue chromosome analysis, Miscarriage chromosome analysis, Spontaneous abortion chromosome analysis, Stillbirth chromosome analysis, Fetal autopsy chromosome analysis, POC karyotyping
Connexin 26 Mutation Analysis (GJB2 Sequencing) Connexin 26
Connexin 26, CX26, GJB2 sequence analysis, Connexin 26 sequencing, Connexin 26 sequence analysis, Pre-lingual hearing loss, Non-syndromic hearing loss, Non-syndromic deafness, DFNB1A, DFNB1, DFNA3A, DFNA3
CSF Cytology with Wet Prep for Amoeba CSF Cytology with Wet Prep for Amoeba
PAM, wet mount, parasite, CSFWPA, Acanthamoeba
CTNNB1 (Beta-Catenin) Exon 3 Sequencing CTNNB1 (Beta-Catenin) Exon 3 Sequencing
CTNNB1 targeted exon sequencing, Beta catenin targeted exon sequencing, CTNNB1 targeted exon sequence analysis, CTNNB, WNT subgroup Medulloblastoma, PNET, Primitive neuroectodermal tumor, Beta-catenin mutation analysis
Culture- Bacterial, Body Fluid Culture, Body Fluid
Bacterial Culture, Body Fluid, Joint Fluid Culture, Knee Fluid Culture, Peritoneal Fluid Culture, Synovial Fluid Culture
Cytology Cytology
DNA Ploidy Analysis DNA Ploidy Analysis
DNA Ploidy Analysis, Ploidy Analysis, DNA, DNA Index
Electrolytes Electrolytes
Electrolytes, Carbon Dioxide (Electrolytes), Chloride (Electrolytes), Cl (Electrolytes), CO2 (Electrolytes), K (Electrolytes), Lytes, Na (Electrolytes), Potassium (Electrolytes), Sodium (Electrolytes)
Enterovirus/Parechovirus by RT-PCR, Qualitative Entero/Parechovirus by PCR
Enterovirus by PCR, Parechovirus by PCR, Enterovirus and Parechovirus by PCR, EV by PCR, PEV by PCR, echoviruses, Coxsackie
Epstein Barr Virus by PCR, Quantitative EBV by PCR, Quant
EBV PCR Quantitative, Quantitative EBV PCR, PCR for EBV Quantitative, EBV Quantitative, Epstein Barr Virus by PCR
Erythrocyte Porphyrin (EP), Whole Blood Erythrocyte Protoporphyrin,Free
Erythrocyte Protoporphyrin, Free, FEP, Protoporphyrins, Free Erythrocyte, Porphyrins (FEP), Protoporphyrin, Free Erythrocyte (FEP), Protoporphyrins, Total, Erythrocytes, RBC Porphyrins, Red Blood Cell Porphyrins
Factor II (Prothrombin) Mutation Factor II (Prothrombin) Mutation
Prothrombin (F2) Mutation , Factor 2 mutation analysis, F2 mutation analysis, Prothrombin (Factor II) mutation analysis, Prothrombin-related thrombophilia, 20210G>A mutation, G20210A mutation, Prothrombin (Factor 2) G20210A mutation PCR
Fatty Acid Profile, Essential, Serum Fatty Acid Profile, Essential, Serum
C12-C22, Fatty Acid Profile, Essential, Essential Fatty Acids, Long-Chain Fatty Acids (LCFA), Omega 3, Omega 6, Omega 7, Omega 9, Omega fatty acids, Soft-FAPEP, Polyunsaturated Fatty Acids, Lauric Acid, Myristic Acid, Hexadecenoic Acid, Palmitoleic Acid, Palmitic Acid, Gamma-Linolenic Acid, Alpha-Linolenic Acid, Linoleic Acid, Oleic Acid, Vaccenic Acid, Stearic Acid, Eicosapentaenoic Acid, Arachidonic Acid, Mead Acid, Homo-Gamma-Linolenic Acid, Arachidic Acid, Docosahexaenoic Acid, Docosapentaenoic Acid, Docosatetraenoic Acid, Docosenoic Acid, Nervonic Acid, Total Lipid Fatty
Fatty Acids, Long Chain Fatty Acids, Long Chain
Long Chain Fatty Acids, Very Long Chain Fatty Acids, Phytanic acids, X-linked Adrenoleukodystrophy, Zellweger Spectrum Disease
FISH Analysis FISH Analysis Only
Metaphase FISH, Constitutional FISH, Microdeletion syndrome, Microduplication syndrome, DiGeorge / Velocardiofacial syndrome (22q11.2), 22q11.2 deletion, Angelman syndrome (15q11.2-13), Prader-Willi syndrome (15q11.2-13), Cri-du-chat (5p-) syndrome (5p15.2), Wolf-Hirschhorn (4p-) syndrome (4p16.3), Williams syndrome (7q11.23), Smith-Magenis syndrome (17p11.2), Kallmann syndrome (Xp22.3), Miller-Dieker syndrome (17p13.3), Steroid sulfatase deficiency (STS) (Xp22.3), X-linked ichthyosis STS deletion, XIST deletion (Xq13.2), SRY detection (Yp11.3), Phelan-McDermid syndrome (22q13.3), Custom FISH analysis, Specialized FISH analysis, FISH for chromosome rearrangement, Chromosome translocation FISH, Chromosome inversion FISH, Marker chromosome FISH, Chromosome insertion FISH, Centromere FISH, Telomere FISH, Microdeletion FISH analysis
FOXO1 (FKHR) Rearrangement Detection, FISH Tumor Analysis FISH Tumor Analysis (FKHR)
FOXO1 FISH, FOXO1A FISH, FKHR FISH, ARMS FISH, Alveolar rhabdomyosarcoma (ARMS) FISH, PAX3/FOXO1A FISH, PAX3-FOXO1A FISH, PAX7/FOXO1A FISH, PAX7-FOXO1A FISH, FKHR break-apart FISH, FOXO1 break-apart FISH, FKHR gene fusion, FOXO1 gene fusion, FOX01, FOXO1, FOXO1A, FOXO1A, FKHR, FOXO1 (13q14) gene rearrangement, FOXO1 rearrangement, FKHR rearrangement, FOXO1 fusion, FKHR fusion, PAX3-FOXO1, PFAX3/FOXO1, PAX7-FOXO1, PAX7/FOXO1
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