Test Menu
PRENATAL DIAGNOSTICS:
- Alpha-fetoprotein (AFP) analysis of amniotic fluid
- Amniocentesis
- Amniocytes for Enzyme Assay
- California Prenatal Screening Program
- Chorionic villus sampling (CVS)
- Comprehensive prenatal testing services
- Nuchal Translucency (NT) Ultrasound
- Prenatal Targeted Array CGH
CYTOGENETIC DIAGNOSTIC TEST MENU:
- Amniotic Fluid and Chorionic Villi Cytogenetic Analysis
- Chromosome breakage studies for Fanconi Anemia
- Fluorescence In Situ Hybridization (FISH) Analysis (test menu)
- Neoplastic Cytogenetics
- Peripheral Blood Cytogenetic Analysis
- Products of conception
- Tumor and Solid Tissue Cytogenetic Analysis
- Skin and other tissue for cytogenic analysis
MOLECULAR DIAGNOSTIC TEST MENU:
- 180K Oligonucleotide Array CGH
- Ashkenazi Jewish Panel:
- Canavan
- Familial Dysautonomia
- Gaucher
- Tay-Sachs
- Connexin 26 (GJB2) Sequence Analysis
- Connexin 26 (GJB2) Targeted Mutation Analysis
- Connexin 30 (GJB6) Targeted Mutation Analysis
- Craniosynostosis Syndrome Comprehensive Testing
- Apert Syndrome
- Comprehensive Craniosynostosis Panel
- Crouzon Syndrome
- Crouzon Syndrome with Acanthosis Nigricans
- FGFR1 Mutation Testing
- FGFR2 Mutation Testing
- FGFR3 Mutation Testing
- Muenke Syndrome
- Non-Syndromic Craniosynostosis
- Pfeiffer Syndrome
- Saethre-Chotzen Syndrome
- Testing for a Known Familial Mutation in FGFR1, FGFR2, FGFR3 or TWIST genes
- Cystic Fibrosis CFTR Full Gene Sequencing
- Cystic Fibrosis Targeted Mutation Panel
- Factor II
- Factor V Leiden
- Fragile X Syndrome
- Hereditary Hemochromatosis
- JAK2 Targeted Mutation Analysis (V617F mutation)
- Methylation studies:
- Angelman syndrome
- Prader-Willi syndrome
- Mitochondrial Common Panel
- Mitochondrial Hearing Loss Sequencing (MT-RNR1 and MT-TS1 genes)
- MTHFR
- Myotonic Dystrophy
- Non-syndromic Hearing Loss:
- Comprehensive Non-Syndrome Hearing Loss Panel
- Connexin 26 Sequence Analysis
- Connexin 26 Targeted Mutation Analysis
- Connexin 30 Targeted Mutation Analysis
- Mitochondrial Hearing Loss Sequencing
- Paternity Testing
- Skeletal Dysplasia Panel
- Specimen Identity Testing
- Spinal Muscular Atrophy
- Thrombotic Risk Panel:
- Factor V Leiden,
- Factor II,
- MTHFR C677T,
- MTHFR A1298C.
For coordination of specimen pick-up and for further information, please contact Genetics Center: 714-288-3500 or
Toll Free: (888) 4-GENETIC
Quality Assurance:
Genetics Center is focused in providing services relating to human genetics. Our executive team is comprised of several physicians with ABMG board certifications in Clinical Genetics, Clinical Molecular Genetics, and Clinical Cytogenetics; PhD Scientists, CLS Certified Laboratory Technicians and Genetic Counselors. Read more.
Genetics Center has been in operation since 1986 in Orange County located in southern California. We offer comprehensive clinical and laboratory services. Genetics Center is certified by the U.S. Department of Health & Human Services, is licensed by the State of California Department of Public Health as a clinical laboratory, and is CLIA and CAP accredited. We are approved by the California State Genetic Disease Branch as a comprehensive prenatal diagnosis center (PDC) and contracted for California Prenatal Screening Program follow-up services. Genetics Center has a training program that is approved by the California Department of Health Services Laboratory Field Services to train Clinical Cytogeneticist Scientists for State licensure and accredited to provide Continuing Education acceptable for that State license. We are also Children’s Oncology Group (COG) approved.
