The Laboratory for Molecular Medicine at Partners HealthCare Personalized Medicine offers genetic testing for various inherited diseases and disorders, as well as, genome sequencing.
To order a test at the LMM, the following is needed:
- A health care provider to order the test (i.e., geneticist, cardiologist, genetic counselor). A patient cannot order a genetic test for him/herself.
- A completed requisition and consent form for the test being ordered (see requisition forms for the disease-specific forms).
- A blood or saliva sample to run the test (see sample requirements).
- Determine how payment for the test will be made (see methods of payment).
Please send the completed requisition and consent form along with the sample to the Laboratory for Molecular Medicine (see shipping).
Once testing is completed, the health care provider will receive a report and discuss the test results.
Hereditary Paraganglioma/Pheochromocytoma Panels
Pan Cardiomyopathy, HCM, DCM, ARVC/CPVT, LVNC Panels
Congenital Heart Defect Panel
Marfan and Loeys-Dietz Syndromes, Familial Thoracic Aortic Aneurysms and Aortic Dissections (TAAD)
X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED), Hidrotic Ectodermal Dysplasia 2 (Clouston Syndrome, GJB2 - Related Ectodermal Dysplasia, DSP - Related Ectodermal Dysplasia / Skin Fragility
Clinical Genome Sequencing
OtoGenome™ Test, Usher Syndrome Panel and other hearing loss related syndromes
Noonan Spectrum Disorder Panel
PulmoGene Panel, Cystic Lung Disease Panel, Bronchiectasis Panel, Basic Fibrosis Panel, Pulmonary Fibrosis - Hermansky-Pudlak Panel, Hermansky-Pudlak Syndrome Panel, Pulmonary Hypertension Panel, Central Hypoventilation Syndrome Panel