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Michigan State University Clinical Genetics Laboratory

GTR Lab ID: 1274, Last updated:2015-03-12
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Conditions and tests

  • 22q11.2 duplication syndrome1 test
  • 46,XX testicular disorder of sex development1 test
  • 46,XY disorder of sex development and 46,XY complete gonadal dysgenesis1 test
  • 4p partial monosomy syndrome1 test
  • 5p partial monosomy syndrome1 test
  • Abnormality of the respiratory system1 test
  • Acute lymphoid leukemia1 test
  • Acute myeloid leukemia2 tests
  • Anaplastic large cell lymphoma1 test
  • Angelman syndrome2 tests
  • Autism spectrum disorders2 tests
  • Azoospermia1 test
  • Burkitt lymphoma1 test
  • Carcinoma of colon2 tests
  • Chronic lymphocytic leukemia1 test
  • Chronic myeloid leukemia1 test
  • Cognitive impairment2 tests
  • Congenital chromosomal disease2 tests
  • Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing1 test
  • Developmental disorder1 test
  • Dysmorphic features2 tests
  • Failure to thrive1 test
  • Follicular lymphoma 11 test
  • Genetic predisposition1 test
  • Hemochromatosis type 11 test
  • Infertility due to oligospermia1 test
  • Kallmann syndrome 11 test
  • Known OR suspected fetal abnormality affecting management of mother1 test
  • Lissencephaly1 test
  • Lymphoid leukemia1 test
  • Male infertility2 tests
  • Malignant lymphoma, large B-cell, diffuse1 test
  • Malignant lymphoma, non-Hodgkin1 test
  • Mantle cell lymphoma1 test
  • Mixed lineage leukemia1 test
  • Mucosa-associated lymphoma1 test
  • Multiple congenital anomalies2 tests
  • Multiple myeloma1 test
  • Myelodysplastic syndrome1 test
  • Myeloid leukemia1 test
  • Myeloproliferative disorder1 test
  • Neoplasm of the breast1 test
  • Non-small cell lung cancer1 test
  • Oligoastrocytoma1 test
  • Oligodendroglioma1 test
  • Prader-Willi syndrome2 tests
  • Pre-B-cell acute lymphoblastic leukemia1 test
  • Secondary leukemia1 test
  • Shprintzen syndrome1 test
  • Smith-Magenis syndrome1 test
  • Sotos syndrome 11 test
  • Spontaneous abortion1 test
  • Williams syndrome1 test
  • X inactivation, familial skewed, 11 test
  • X inactivation, familial skewed, 21 test

List of services

  • Genetic counseling
  • Insurance billing
  • Marker Chromosome Identification
  • Result interpretation
  • X-Chromosome Inactivation Studies

List of certifications/licenses


  • CLIAHelp, Number: 23D0650879, Expiration date: 2016-08-20

Participation in external programs

Standardization programs

  • ISCA Consortium (International Standards for Cytogenomic Arrays)

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.

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