Navigation

Navigation
You are here: Home > Labs Directory > Molecular Pathology
Document Actions

Molecular Genetics Laboratory

by mike_rogers — last modified November 09, 2009 05:00 PM


UNC Hospitals
McLendon Clinical Laboratories
101 Manning Drive
Chapel Hill, NC 27514
 
McLendon Clinical Laboratories
Molecular Genetics Laboratory
Location: 1031 East Wing, UNC Hospitals
Phone: (919)966-4408
FAX: (919)966-6351

Director of Molecular Pathology Program

Director of Molecular Genetics Laboratory,
Associate Director of Molecular Pathology Program

Scientific Director of Molecular Genetics Laboratory,
Associate Director of
Molecular Pathology Program

Margaret L. Gulley, MD

Karen Weck, MD

Jessica Booker, PhD

843-4595

966-4408

966-4408

 

Faculty and Attending Pathologists

Leigh Thorne, MD, Director of Molecular Oncology

William Funkhouser, Jr., MD, PhD

Rosann Farber, PhD

Maimoona Zariwala, PhD

 

 

Assistant Administrative Director

Supervisor

Kim Wait, MT(ASCP)

Howard Parker, MT(ASCP)

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 Mutation Test in Colorectal 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
  • Cystic Fibrosis (CFTR) mutation panel pdf file
  • EBV Viral Load for Epstein-Barr virus 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
  • 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
  • Microsatellite Instability Testing in Colon and Endometrial Cancer 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

    Laboratory Test List Information:
    • UNC Molecular Genetics Laboratory Test Menu pdf file

      Laboratory Request Forms:
    • Molecular Genetics Test Request: Form
      • Directions for Collecting and Mailing Specimens for Molecular Testing pdf file
  •  
     
    Site-wide Actions
    Personal tools