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GTR Home > Laboratories > Molecular Genetics Laboratory

Molecular Genetics Laboratory

GTR Lab ID: 1036, Last updated:2024-07-23

Personnel

  • Director: Hong Wang, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
    Phone: 416-756-6796
    Fax: 416-756-6792
    Email: hong.wang@nygh.on.ca
  • Marit Skuterud, Staff
    Phone: 1-416-756-6444 ext 3500
    Fax: 416-756-4729
    Email: marit.skuterud@nygh.on.ca

Conditions and tests

  • Acute myeloid leukemia1 test
  • Acute promyelocytic leukemia1 test
  • AIP-Related Familial Isolated Pituitary Adenomas1 test
  • Amyotrophic lateral sclerosis1 test
  • APC-related attenuated familial adenomatous polyposis4 tests
  • Ashkenazi Jewish disorders1 test
  • AXIN2-related attenuated familial adenomatous polyposis1 test
  • Azorean disease1 test
  • BAP1-related tumor predisposition syndrome2 tests
  • Basal cell nevus syndrome 11 test
  • Basal cell nevus syndrome 21 test
  • Breast cancer, susceptibility to2 tests
  • Carcinoma of male breast2 tests
  • Carney complex, type 11 test
  • Carney-Stratakis syndrome1 test
  • Colorectal cancer4 tests
  • Comprehensive testing for inherited renal disease1 test
  • Congenital chromosomal disease2 tests
  • Cowden syndrome3 tests
  • Dentatorubral-pallidoluysian atrophy1 test
  • Dizygotic twins1 test
  • Endometrial cancer2 tests
  • Familial adenomatous polyposis 11 test
  • Familial adenomatous polyposis 21 test
  • Familial adenomatous polyposis 32 tests
  • Familial melanoma1 test
  • Familial meningioma1 test
  • Familial multiple polyposis syndrome3 tests
  • Familial pancreatic carcinoma1 test
  • Familial primary hyperparathyroidism1 test
  • Familial prostate cancer3 tests
  • Familial spontaneous pneumothorax1 test
  • Fluorouracil response1 test
  • Fragile X syndrome1 test
  • Fragile X-associated tremor/ataxia syndrome1 test
  • Friedreich ataxia 11 test
  • Frontotemporal dementia1 test
  • Gastric cancer3 tests
  • Gastrointestinal stromal tumor1 test
  • Glioma susceptibility1 test
  • Glioma susceptibility 11 test
  • Glioma susceptibility 21 test
  • Gorlin syndrome1 test
  • Hematologic neoplasm1 test
  • Hemochromatosis type 11 test
  • Hepatocellular carcinoma1 test
  • Hereditary breast ovarian cancer syndrome3 tests
  • Hereditary cancer-predisposing syndrome18 tests
  • Hereditary diffuse gastric adenocarcinoma3 tests
  • Hereditary leiomyomatosis and renal cell cancer2 tests
  • Hereditary mixed polyposis syndrome3 tests
  • Holoprosencephaly 71 test
  • Huntington disease1 test
  • Huntington disease-like syndrome due to C9ORF72 expansions1 test
  • Ischemic stroke1 test
  • Juvenile Polyposis3 tests
  • Kennedy disease1 test
  • Li-Fraumeni syndrome2 tests
  • Lynch syndrome5 tests
  • Lynch syndrome 11 test
  • Medulloblastoma1 test
  • Melanoma1 test
  • Melanoma, cutaneous malignant, susceptibility to, 21 test
  • Melanoma, cutaneous malignant, susceptibility to, 31 test
  • Microcephaly, normal intelligence and immunodeficiency1 test
  • Mismatch repair cancer syndrome 11 test
  • Mismatch repair cancer syndrome 21 test
  • Mismatch repair cancer syndrome 31 test
  • Mismatch repair cancer syndrome 41 test
  • Multiple endocrine neoplasia, type 11 test
  • Multiple endocrine neoplasia, type 21 test
  • Myelodysplastic syndrome1 test
  • Myeloproliferative neoplasm1 test
  • Neurofibromatosis, familial spinal1 test
  • Neurofibromatosis, type 12 tests
  • Neurofibromatosis, type 21 test
  • Nonpapillary renal cell carcinoma2 tests
  • Oculopharyngeal muscular dystrophy1 test
  • Ovarian cancer2 tests
  • Ovarian small cell carcinoma1 test
  • Pancreatic adenocarcinoma2 tests
  • Papillary renal cell carcinoma type 11 test
  • Paragangliomas 11 test
  • Paragangliomas 22 tests
  • Paragangliomas 31 test
  • Paragangliomas 41 test
  • Paragangliomas 52 tests
  • Peutz-Jeghers syndrome3 tests
  • Pheochromocytoma1 test
  • Pleuropulmonary blastoma1 test
  • Polyposis syndrome, hereditary mixed, 22 tests
  • Premature ovarian failure 11 test
  • PTEN hamartoma tumor syndrome1 test
  • Retinoblastoma1 test
  • Rhabdoid tumor predisposition syndrome1 test
  • Rhabdomyosarcoma, embryonal, 21 test
  • Schwannomatosis1 test
  • Schwannomatosis 12 tests
  • Schwannomatosis 22 tests
  • Sessile serrated polyposis cancer syndrome3 tests
  • Soft tissue sarcoma1 test
  • Spinocerebellar ataxia 71 test
  • Spinocerebellar ataxia type 11 test
  • Spinocerebellar ataxia type 171 test
  • Spinocerebellar ataxia type 21 test
  • Spinocerebellar ataxia type 61 test
  • Spinocerebellar ataxia type 81 test
  • Thrombophilia due to activated protein C resistance1 test
  • Tuberous sclerosis 12 tests
  • Tuberous sclerosis 22 tests
  • Tuberous sclerosis syndrome1 test
  • Von Hippel-Lindau syndrome2 tests
  • Y chromosome deletions1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Deletion/Duplication Testing
  • Custom Sequence Analysis
  • Custom microarray analysis
  • Carrier testing
  • Identity Testing
  • Maternal cell contamination study (MCC)
  • Uniparental Disomy (UPD) Testing

List of certifications/licenses

Certifications

  • Ministry of Health Long Term Care (MOHLTC), Number: 4047, Expiration date: 2025-04-29

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.