Molecular Genetics Laboratory
Last modified by
IMarrero
on
March 13, 2012 12:41 PM
|
UNC Hospitals McLendon Clinical Laboratories 101 Manning Drive Chapel Hill, NC 27514 |
Molecular
Genetics Laboratory
Location: 1031 East Wing, UNC Hospitals
Phone: (919)966-4408
FAX: (919)966-6351
Location: 1031 East Wing, UNC Hospitals
Phone: (919)966-4408
FAX: (919)966-6351
|
Director of Molecular Pathology Program |
Director of Molecular Genetics
Laboratory, |
Scientific Director of Molecular
Genetics Laboratory, |
|
843-4595 |
966-4408 |
966-4408 |
|
Faculty and Attending Pathologists |
|
Leigh Thorne, MD, Director of Molecular Oncology |
|
Assistant Administrative Director |
Supervisor |
|
966-8452 |
843-0401 |
- The Molecular Genetics Laboratory performs the following
clinical molecular tests:
- Click on underlined pdf file for additional information
.
-
- Alpha-1 Antitrypsin Z and S Mutations pdf file
- BRCA 1/2 gene mutations for breast cancer predisposition Test information
- BCR/ABL1 for leukemia pdf file
- BCR-ABL1 Gleevec Resistance pdf file
- BK Polyomavirus Viral Load Quantitative PCR Assay pdf file
- BRAF V600E gene mutation test in cancer pdf file
- CMV viral load for cytomegalovirus pdf file
- Congenital CMV Assay on Dried Blood from Perinatal Cards pdf file
- Connexin 26 (GJB2) and connexin 30(GJB6) for hearing loss pdf file
- CYP2C19 Sequence Variants Associated with Resistance to Clopidogrel(Plavix) pdf file
- Cystic Fibrosis (CFTR) mutation panel pdf file
- EBV Viral Load for Epstein-Barr virus pdf file
- EGFR Mutation Associated with Drug Response pdf file
- Extract and hold DNA or RNA DNA Test information RNA Test information
- DNA Fingerprinting, for marrow engraftment pdf file
- Factor V Leiden for venous thrombosis pdf file
- Factor II(Prothrombin) mutation for venous thrombosis pdf file
- FLT3 and NPM1 Gene Defects Refine Prognosis of Acute Myelogenous Leukemia pdf file
- Fragile X Syndrome of Mental Retardation pdf file
- Gene Expression Profiling of Frozen Tumors for Clinical Trials pdf file
- Hemochromatosis, (HFE gene) pdf file
- IDH1 & IDH2 Mutation in Glial Lesions and Myeloid Malignancy pdf file
- JAK2 1849G>T[V617F] Mutation in Chronic Myeloproliferative Disorders pdf file
- KIT Mutations Conferring Drug Susceptability pdf file
- KRAS mutation for colon or lung cancer drug resistance pdf file
- MCAD Deficiency, medium chain acyl CoA dehydrogenase pdf file
- MGMT Promoter Methylation Conferring Sensitivity to Alkylating Agents pdf file
- MGMT Promoter Methylation Test Predicts Drug Effect in Glioblastoma pdf file
- Microsatellite Instability Testing in Colon and Endometrial Cancer pdf file
- MLH1 Promoter Hypermethylation pdf file
- Molecular Test for Mitochondrial DNA 1555A>G Mutation Associated with Aminoglycoside-induced and Non-syndromic Hearing Loss pdf file
- Prader Willi or Angelman Syndrome pdf file
- Primary Ciliary Dyskinesia/Kartagener Syndrome(PCD), testing for DNAI1 and DNAH5 mutations pdf file and PCD test information
- PCD Foundation brochure pdf file
- PCD Clinical History Form pdf file
- T- & B-cell Clonality for lymphoid lesions pdf file
- UGT1A1 Genotype Predicts Irinotecan Toxicity or Confirms Gilbert's Syndrome pdf file
- Validating Molecular Assays for Use in Clinical Trials
pdf file
Laboratory Test List Information:
