Quest Diagnostics
The Industry Leader in Genetic Testing
Why Choose Quest Diagnostics for Your Genetics Testing?
| • | Innovation – Quest Diagnostics is the first national clinical laboratory to offer testing for the entire Cystic Fibrosis (CF) gene sequence, with CF Complete.™ |
| • | Comprehensive Menu – Full range of prenatal testing including both screening and diagnostic tests (pre-and postnatal). With a broad menu of genetic tests and a tradition of innovation, Quest Diagnostics is committed to the development of groundbreaking genetic testing services for you and your patients |
| • | Expertise – Availability of consultations with Board certified Scientific and Medical Directors, Genetic Counselors and Academic Associates. |
Services for Physicians
Quest Diagnostics Genetics Center
For physicians requiring assistance with maternal serum screening results or with a specific technical question regarding biochemical, cytogenetics, or molecular testing, a dedicated genetics customer service professional will answer your questions or, if appropriate, connect you with one of our:
| • | Seventeen Directors certified by the American Board of Medical Genetics, |
| • | Eight genetic counselors certified by the American Board of Genetic Counseling, or |
| • | Two academic associates (thought leaders from academic medical centers). |
These technical experts will be glad to provide you with advice and service in any of the following areas:
| • | Recalculation of maternal serum screening results |
| • | Scientific and medical consultation |
| • | Specimen requirements |
| • | Assay set-up and results schedules |
| • | Test results |
With four premier laboratories, the Quest Diagnostics Genetics Center is at the forefront of genetic testing. Locations include:
| • | San Juan Capistrano, California (Nichols Institute) |
| • | Chantilly, Virginia (Nichols Institute) |
| • | Van Nuys, California |
| • | Teterboro, New Jersey |
Contact the Quest Diagnostics Genetics Center toll-free, at
Biochemical Genetics
Pediatric
| • | Amino Acid Analysis, Qualitative |
| • | Amino Acid Analysis, Quantitative |
| • | Congenital Adrenal Hyperplasia (CAH) |
| • | Inborn Errors of Metabolism, Basic Screen |
| • | Organic Acids, Quantitative, Full Panel |
Prenatal
| • | Maternal Serum Screen, First Trimester |
| • | Maternal Serum Screen 4 (Quad Screen) |
| • | Maternal Serum Screen 5 (Penta Screen) |
Cytogenetics
| • | Chromosome Analysis |
| • | Fluorescent in-situ hybridation |
| • | Chromosome Rearrangement, SKY™ (Spectral Karyotyping) |
Molecular Genetics
Prenatal/Carrier Testing
| • | Ashkenazi Jewish Panel Test Bulletin |
| • | Cystic Fibrosis Test Menu |
| • | Cystic Fibrosis Test Summary & Mutation List |
| • | Cystic Fibrosis Complete™ Gene Sequencing Assay Test Bulletin |
Coagulation Testing
| • | Factor V (Leiden) Mutation Analysis |
| • | Prothrombin (Factor II) 20210G<A Mutation Analysis |
| • | Methylenetetrahydrofolate Reductase (MTHFR) Mutation |
Online Test Information for Your Patients
Your patients can learn about health conditions and laboratory tests in our online Patient Health Library. The library is founded on evidence-based information, and includes topics such as:
Contact a Quest Diagnostics Sales Representative,
learn more about our testing services, and become a client
| • | Contact a physician sales representative |
| • | Contact a hospital sales representative or learn about our complete hospital offerings |
