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- Acylcarnitine Profile
- (3MCC) – MCCC1/MCCC2 Sequencing
- Aarskog Syndrome (FGD1) Sequencing
- Allan-Herndon-Dudley Syndrome (MCT8) Sequencing
- Alpha-Mannosidosis (MAN2B1) Sequencing
- Lysosomal Enzyme Panel
- Alpha-Thalassemia X-linked Intellectual Disability (ATR-X) Sequencing
- Amino Acids - Quantitative
- Aminoglycoside-induced Hearing Loss
- Angelman Syndrome (UBE3A) sequencing
- ARX-related Spectrum of X-Linked Intellectual Disability Gene Sequencing
- Biochemical Genetics Profile
- Biotinidase Deficiency
- Biotinidase Deficiency (BTD) Sequencing
- Glutarylcarnitine (C5-DC)
- Cardio-Facio-Cutaneous (CFC) Syndrome – Tiered Molecular Testing
- Carnitine Analysis, Total and Free
- CASK-related Intellectual Disability
- CDKL5-related Atypical Rett Syndrome (STK9) Sequencing
- CHARGE syndrome (CHD7) Sequencing
- Christianson Syndrome/X-linked Angelman-like Syndrome
- Chromosome Studies - Special Stains
- Prenatal Chromosome Analysis – Amniotic Fluid
- Prenatal Chromosome Analysis – Chorionic Villus Sampling (CVS)
- Peripheral Blood Chromosome Analysis
- Cytogenetic Analysis of Solid Tissue
- Citrullinemia Type 1 (ASS1)
- Coffin-Lowry Syndrome (RSK2) Sequencing
- Congenital Disorder of Glycosylation Ia (PMM2) Sequencing
- Congenital Disorder of Glycosylation Ib (MPI) Sequencing
- Congenital Rett Syndrome Variant (FOXG1)
- Congenital Disorder of Glycosylation Ic (ALG6) Sequencing
- Connexin 26 (GJB2) Sequencing
- Copper Transport Disorders (ATP7A sequencing)
- Costello Syndrome – Tiered Molecular Testing
- CPT1A Sequencing
- Creatine Transporter Deficiency (SLC6A8) Sequencing
- Creatine Transporter Deficiency – Biochemical Analysis
- Creatine/GAA (guanidinoacetate) – Creatine Biosynthesis Disorders
- Cystic Fibrosis (CFTR) Mutation Panel
- DCX-Related Disorders
- Duchenne and Becker Muscular Dystrophy (DMD) MLPA
- Early Infantile Epileptic Encephalopathy 4
- Fibroblast Growth Factor Receptor 2 (FGFR2)-related Craniosynostosis
- FISH for Congenital Anomalies
- Fibroblast Growth Factor Receptor 3 (FGFR3)-related Skeletal Dysplasias
- Fragile X syndrome (FMR1)
- FRAXE syndrome (FMR2)
- Galactose-1-Phosphate
- Classical Galactosemia (GALT) Sequencing
- Greig Cephalopolysyndactyly, Pallister-Hall Syndrome
- Glutaric Acidemia, Type I (GCDH) Sequencing
- Hematological Disease Studies – FISH Panels and Specific Probes
- Hemochromatosis (HFE) Mutation Analysis
- Hunter Syndrome (IDS) Sequencing
- Hunter Syndrome – Enzyme Analysis
- Hurler syndrome (IDUA) Sequencing
- Hydrops Panel – Enzyme Analysis
- Kabuki Syndrome
- Kallmann Syndrome 5 (CHD7) Sequencing
- LEOPARD Syndrome – Tiered Molecular Testing
- Marfan Syndrome (FBN1) Sequencing
- Maroteaux Lamy syndrome - Enzyme Analysis
- Maroteaux-Lamy syndrome (ARSB) Sequencing
- MCAD Deficiency (ACADM) sequencing
- MED12-related syndromes
- Metabolic Screen - Urine
- Metachromatic Leukodystrophy – Enzyme Analysis
- Morquio A, MPS IA (GALNS) Sequencing
- Morquio syndrome, Types A and B - Enzyme Analysis
- Mucolipidosis II/III (Plasma Screen)
- Mucolipidosis II/IIIA (GNPTAB) Sequencing
- Mucopolysaccharide Analysis
- Mucopolysaccharidosis Enzyme Panel
- Myotonic Dystrophy
- Noonan Syndrome – Tiered Molecular Testing
- Oligosaccharides
- Organic Acids
- Orotic Acid
- Ornithine transcarbamylase deficiency
- TP63/p63-related Syndromes – Selected Exons
- X-linked Female-Limited Epilepsy with ID (PCDH19 sequencing)
- Phenylketonuria (PAH) Sequencing
- Borjeson-Forssman-Lehmann syndrome
- Pitt-Hopkins Syndrome (TCF4) Sequencing
- Pelizaeus-Merzbacher Disease (PLP1 Sequencing)
- POLG1-related Disorders - Sequencing
- Pompe disease (Glycogen Storage Disease Type II) - Enzyme Analysis
- Prader-Willi/Angelman Methylation Studies
- Prenatal Screening – Maternal Serum Screening/Quad Screen
- Primary Carnitine Deficiency (SLC22A5) Sequencing
- PTEN-related syndromes – PTEN sequencing
- Rett syndrome (MECP2) Sequencing and MLPA
- Rett/Angelman Syndrome 2nd Tier Sequencing Panel
- Saethre-Chotzen Syndrome (TWIST) Sequencing and MLPA
- Sanfilippo Syndrome Panel – Enzyme Analysis
- Sanfilippo Syndrome - Type A - SGSH sequencing
- Sialic Acid
- Storage Disease Panel
- Transferrin Isoelectric Focusing – CDG screening
- Whole Genome SNP Microarray
- X-Chromosome High Density Array
- FLNA-related disorders, sequencing
- Fucosidosis (FUCA1) Sequencing
- GM1 gangliosidosis (GLB1) Sequencing
- Galactosialidosis, CTSA sequencing
- Morquio B, MPS IVB (GLB1) Sequencing
- Uniparental Disomy (UPD) Studies
- Syndromic Autism Panel
- X-I Studies
- NGS Connective Tissue Panel
- NGS Skeletal Dysplasia Panel
- Dried Blood Spot Lysosomal Enzyme Panel
- Sotos syndrome (NSD1)
- NGS Epilepsy/Seizure Panel
- L1CAM sequencing
- Beckwith-Wiedemann syndrome
- Russell-Silver syndrome (11p15.5)
- Gaucher Disease (GBA) Sequencing
- Sanfilippo B (NAGLU) sequencing
- Krabbe Disease (GALC) Sequencing & Del/Dup
- NGS XLID panel
- ACSL4
- NGS Non-immune Hydrops
- Sanfilippo B (NAGLU) sequencing (2)
- Niemann Pick A/B (SMPD1) sequencing
- Wolman Disease Enzyme
- Oligosaccharidoses enzyme panel
- Neurological Enzyme Panel
- Keratan Sulfate - urine (uKS)
- SCOT Deficiency
- Batten Disease
- SCAD
- NGS CDG Panel
- NGS Craniosynostosis Panel
- NGS NCL Panel
- NGS Peroxisome Biogenesis Panel
- CPT2 sequencing
- Glycogen Synthase Deficiency Seq
- Cornelia de Lange
- NGS Overgrowth/Macrocephaly Panel
- NGS Hearing Loss Panel
- LSD NBS Screening Follow-up
- Whole Exome Sequencing (WES)
- NGS Aortic Dysfuntion or Dilation and Related Disorders Panel
- NGS RASopathy Panel
- NGS Rhabomyolysis and Metabolic Myopathies Panel
- NGS Vascular Disorders Panel
- NGS Lysosomal Storage Diseases Panel
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