| TEST |
FEE |
| Achondroplasia |
$307.00 |
| Alpha-thalassemia |
$334.00 |
| Angelman Syndrome (Methylation Analysis - proband only) |
$311.00 |
| Angelman Syndrome (Segregation Analysis- parents and proband) |
$588.00 |
| Apert Syndrome |
$391.00 |
| Beckwith-Wiedemann Syndrome Methylation Analysis and Uniparental Disomy Analysis |
$588.00 |
| Beta-thalassemia Mutation Screening |
$339.00 |
| BCR-ABL Fusion Gene Transcript Detection - Quantitative |
$307.00 |
| Charcot-Marie-Tooth Type 1A |
$391.00 |
| Congenital Adrenal Hyperplasia/21-Hydroxylase Deficiency |
$391.00 |
| Coronoal Craniosynostosis (FGFR2 and FGFR3 Gene sequencing) |
$391.00 |
| Crouzon Syndrome |
$391.00 |
| Cystic Fibrosis (ACOG/ACMG panel) |
$184.00 |
| Dentatorubral-Pallidoluysian Atrophy/Haw River Syndrome |
$229.00 |
| Duchenne/Becker Muscular Dystrophy (Multiplex Deletion Analysis |
$457.00 |
| Duchenne/Becker Muscular Dystrophy (Linkage Analysis) |
$358.00 / sample |
| DNA Banking |
$108.00 |
| Factor V (Leiden) |
$131.00 |
| Fragile X Syndrome |
$274.00 |
| Friedreich's Ataxia |
$296.00 |
| Galactosemia |
$258.00 |
| Hemochromatosis |
$197.00 |
| HELLP Syndrome (Long Chain Acyl-CoA Dehydrogenese Deficiency) |
$131.00 |
| Hemophilia A / Factor VIII Deficiency |
$300.00 |
| Hemoglobin C |
$129.00 |
| Hemoglobin S |
$129.00 |
| Hereditary Neuropathy with Liability to Pressure Palsies |
$391.00 |
| Huntington's Disease |
$229.00 |
| Hyperekplexia (GLRA1) exon 6 gene sequencing |
$435.00 |
| Hypochondroplasia |
$307.00 |
| Long Chain Acyl-CoA Dehydrogenese Deficiency (HELLP Syndrome) |
$131.00 |
| Leber's Hereditary Optic Neuropathy |
$391.00 |
| Machado-Joseph Disease |
$229.00 |
| Medium Chain Acyl-CoA Dehydrogenese Deficiency |
$131.00 |
| Molecular Fingerprinting |
$196.00 / sample |
| Muenke Syndrome (FGFR 3) |
$258.00 |
| Multiple Endocrine Neoplasia Type 2A and 2B/ Familial Medullary Thyroid Carcinoma |
$373.00 |
| Myotonic Dystrophy |
$296.00 |
| Neonatal Hypotonia Screen |
$652.00 |
| Paternity Testing |
($325.00 for alleged father, one child with or without mother) |
| Polyhydramnios Panel |
$652.00 |
| Prader-Willi Syndrome (Methylation Analysis - proband only) |
$311.00 |
| Prader-Willi Syndrome (Segregation Analysis- parents and proband) |
$391.00 |
| RhD Antigen Typing |
$160.00 |
| RhC/c Antigen Typing |
$160.00 |
| Russell-Silver Syndrome Methylation Analysis and Uniparental Disomy Analysis |
$588.00 |
| Sexing |
$258.00 |
| Sickle Cell Anemia |
$129.00 |
| Skeletal Dysplasia Panel (FGFR 3) |
$391.00 |
| Spinobulbar Muscular Atrophy / Kennedy's Disease |
$229.00 |
| Spinocerebellar Ataxia Type 1 |
$229.00 |
| Spinocerebellar Ataxia Type 2 |
$229.00 |
| Spinocerebellar Ataxia Type 3 |
$229.00 |
| Spinocerebellar Ataxia Type 6 |
$229.00 |
| Spinocerebellar Ataxia Type 7 |
$229.00 |
| Spinocerebellar Ataxia Type 8 |
$229.00 |
| Spinocerebellar Ataxia Type 10 |
$229.00 |
| Spinal Muscular Atrophy Types I/II/III (carrier testing available) |
$311.00 |
| Thanatophoric Dysplasia (FGFR3) (TD1 and TD2) |
$391.00 |
| Thrombosis Panel (Factor V, MTHFR, Prothrombin) |
$358.00 |
| Uniparental Disomy Studies |
$196.00 / sample |
| Williams Syndrome (Segregation Analysis - parents and proband) |
$311.00 |
| Zygosity Testing |
$196.00 / sample |
to obtain sample collection and shipping guidelines.