A B C D E F G H I
J K L M N O P Q R
S T U V W X Y Z #
Allergens
Search Site:
 

PAML
110 West Cliff Avenue
Spokane, WA 99204

SWITCHBOARD
Phone: 509.755.8600
Toll Free: 800.541.7891

CLIENT SERVICES 
Phone: 509.755.8999
Toll Free: 800.349.8586
Fax: 509.924.5127

PROVIDERHOSPITALPATIENTJOINT VENTURESDRUG TESTINGCAREERSABOUT US

Molecular Diagnostics

CONTACT INFORMATION

Phone: 509.755.8999 
Toll Free: 800.349.8586
Fax: 509.924.5127

Staffed 24 hours a day, 365 days a year

Technical Directors: Marcy Hoffmann, PhD; Danbin Xu, MD, PhD

PAML offers a wide range of molecular-based technologies to improve patient care by providing highly sensitive and specific testing and timely result reporting.

Molecular testing makes it possible not only to diagnose specific genetic, pathogenic,  and oncologic diseases but also to monitor a patient’s disease over time, a feature that allows for timely patient management and treatment decisions. Furthermore, molecular genetic testing provides highly accurate negative-predictive values when screening for genetic mutations in cystic fibrosis and other diseases.

PAML’s molecular diagnostics laboratory offers DNA storage capabilities.

We also offer nucleic acid-based testing for the diagnosis of select genetic, infectious disease and oncologic anomalies including:

Genetics KRAS - Mutation Detection By Sequence Analysis, Codons  
  Inherited thrombophilia (factor V Leiden and prothrombin or factor II mutations)Test 1  
  Inherited thrombophilia (factor V Leiden and prothrombin or factor II mutations)Test 2  
  Hereditary hemochromatosis (C282Y, H63D and S65C mutations)  
  Cystic fibrosis (32 mutations) TEST UPDATE!
  Fragile X syndrome TEST UPDATE!
  Hereditary hearing loss (connexin 26 sequence analysis) TEST UPDATE!
  MTHFR (C677T and A1298C mutations) TEST UPDATE!
  Spinal muscular atrophy TEST UPDATE!
  Rett syndrome  
Infectious Disease Bordetella pertussis and Bordetella parapertussis  
  Hepatitis B DNA quantification  
   
   
Oncology JAK2 V617F mutation for myeloproliferative disease  
  BCR/ABL1 t(9;22) translocation, qualitative and quantitative  

We provide a full range of molecular diagnostic and consulting services for adult, pediatric, and prenatal cases. We are committed to provide the highest quality of patient care and serve as competent and easily available consultants to our referring physicians. The molecular diagnostics laboratory staff includes a board-certified medical geneticist, who is available for consultation.

Roche Diagnostics
PAML has a strategic alliance with Roche Diagnostics, the world’s leading diagnostics company. PAML, together with Roche, has established a Molecular Center of Excellence (MCOE) for molecular diagnostics and other advanced genomic technologies. Access to Roche’s vast resources has helped PAML bring this emerging technology to our healthcare communities.

 

Privacy Policy   |   HIPAA   |   Disclaimer   |   Contact Us   |  ©2012 PAML