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GTR Home > Laboratories > Medical Genomics Laboratory

Medical Genomics Laboratory

GTR Lab ID: 221768, Last updated:2023-06-07


  • Director: Yulong Fu, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
    Phone: 205-934-5562
    Fax: 205-996-2929
    Email: yulongfu@uabmc.edu
  • Bryce Brown, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 205-934-5525
    Fax: 205-996-2929
    Email: ebfincher@uabmc.edu
    Contact note: 205-934-5562
  • Francine Jones, Office Associate
    Phone: 205-934-5562
    Fax: 205-996-2929
    Email: frjones@uabmc.edu
  • Ryan Lauterbach, BS, Genetic Counselor Assistant
    Phone: 205-934-7387
    Fax: 205-966-2929
    Email: rlauterbach@uabmc.edu
    Contact note: medgenomics@uabmc.edu
  • Brandon Shaw, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 205-934-1520
    Fax: 205-966-2929
    Email: brandonshaw@uabmc.edu
    Contact note: medgenomics@uabmc.edu
  • Ying Wang, MS, MBA, Laboratory Manager
    Phone: 205-934-9889
    Fax: 205-996-2929
    Email: yingw@uab.edu
    Contact note: 205-934-5562

Conditions and tests

  • Atypical teratoid rhabdoid tumor2 tests
  • Bannayan-Riley-Ruvalcaba syndrome1 test
  • Cafe au lait spots, multiple1 test
  • Capillary malformation-arteriovenous malformation syndrome2 tests
  • Cardiofaciocutaneous syndrome 12 tests
  • Costello syndrome2 tests
  • Familial meningioma1 test
  • Fragile X syndrome1 test
  • Juvenile myelomonocytic leukemia2 tests
  • Legius syndrome5 tests
  • Macrocephaly-autism syndrome1 test
  • Malignant rhabdoid tumor, somatic2 tests
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Meningioma1 test
  • Neurofibromatosis, familial spinal3 tests
  • Neurofibromatosis, type 18 tests
  • Neurofibromatosis, type 27 tests
  • Neurofibromatosis-Noonan syndrome2 tests
  • Noonan syndrome2 tests
  • Noonan syndrome with multiple lentigines2 tests
  • Noonan syndrome-like disorder with loose anagen hair2 tests
  • Parkes Weber syndrome2 tests
  • Proteus syndrome1 test
  • Proteus-like syndrome1 test
  • PTEN hamartoma tumor syndrome1 test
  • Rhabdoid tumor1 test
  • Rhabdoid tumor predisposition syndrome 12 tests
  • Rhabdoid tumor predisposition syndrome 22 tests
  • Schwannomatosis1 test
  • Schwannomatosis 15 tests
  • Schwannomatosis 21 test
  • Schwannomatosis-1, susceptibility to1 test
  • Tuberous sclerosis 11 test
  • Tuberous sclerosis 21 test
  • Tuberous sclerosis syndrome1 test
  • Von Hippel-Lindau syndrome1 test

List of services

  • Insurance billing
  • Insurance preverification
  • Biopsy-based/mosaicism analysis
  • Clinical Testing/Confirmation of Mutations Identified Previously: Order Code: KT2
  • Custom Deletion/Duplication Testing: Order Code: KT2
  • Custom Sequence Analysis: Order Code: KT2
  • Carrier testing: Order Code: KT2 or KT2-NG
  • Prenatal testing: Order Code: PT2
  • Maternal cell contamination study (MCC): Order Code: PT2

List of certifications/licenses


  • CLIAHelp, Number: 01D0301478, Expiration date: 2023-11-28
  • CAP, Number: 1544506, Expiration date: 2025-02-05


  • CA - California Department of Public Health CDPH, Number: CDS-90006628, Expiration date: 2024-04-27
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1517
  • PA - Pennsylvania Department of Health PADOH, Number: 33933, Expiration date: 2023-08-15

Participation in external programs

Standardization programs

  • Locus-specific Databases
  • Mutation-specific Databases

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.