- (NIPT) Confirmation
- About Us
- Assure your patients with confidence
- Billing
- Chromosome Testing
- Client Services
- Contact Us
- Diagnostic Services
- Down syndrome (trisomy 21)
- Edwards syndrome (Trisomy 18)
- Employment
- General Information
- Genetic Counseling
- Genetic Disorders Info
- Genetic Disorders Information
- Genetic Testing Laboratory
- Infertility
- Infertility Menu
- Infertility test menu
- Molecular testing
- Non-invasive Prenatal Testing
- Notice of Information
- Oncology
- Oncology Menu
- Oncology test menu
- Patau Syndrome (trisomy 13)
- Pediatric
- Pediatric Menu
- Pediatric test menu
- Practices
- Prenatal
- Prenatal Menu
- Acetylcholinesterase (AChE)
- Alpha-fetoprotein (AF-AFP)
- Amniotic Fluid Chromosome Analysis
- AneuVysion™ Prenatal FISH (13, 18, 21, X, Y) [FDA Approved]
- Assure SNP Microarray Analysis (FDA cleared) – Prenatal & Postnatal
- Chorionic Villus Sampling (CVS) Chromosome Analysis
- Cri-du-chat Syndrome
- DiGeorge/Velocardiofacial Syndrome
- Fragile X Syndrome Testing
- Kallmann Syndrome 1 (KAL1)
- Miller-Dieker Syndrome (MDS)
- Prader-Willi Syndrome (PWS)/Angelman Syndrome
- Smith-Magenis Syndrome
- Steroid Sulfatase Deficiency
- Williams Syndrome
- Wolf-Hirschhorn Syndrome
- Prenatal Test Menu
- Privacy Policy
- Publications
- Requisitions & Forms
- Resource Information
- FAB Classification for Chronic Myeloproliferative Disorders
- FAB Classification of the Myelodysplastic Syndromes
- French-American-British (FAB) Classification of ALL
- French-American-British (FAB) Classification of AML
- Prevalence of Cystic Fibrosis Mutations Chart
- WHO Classification of Malignant Hematological Diseases
- Resource Links
- Services
- Site Map
- Supply requisition
- Terms and Conditions of Use
- Why Choose CytoGenx