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GTR Home > Laboratories > Genetics and Genomic Medicine Centre

Genetics and Genomic Medicine Centre

GTR Lab ID: 506799, Last updated:2024-08-29

Personnel

Conditions and tests

  • Attention deficit hyperactivity disorder1 test
  • Becker muscular dystrophy1 test
  • Cardiofacioneurodevelopmental syndrome1 test
  • Cataract 11 with microphthalmia and neurodevelopmental abnormalities1 test
  • Duchenne muscular dystrophy1 test
  • Epilepsy1 test
  • Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination1 test
  • Neurodevelopmental disorder with hypotonia, seizures, and absent language1 test
  • Neurodevelopmental disorder with motor and speech delay and behavioral abnormalities1 test
  • Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features1 test
  • Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures1 test
  • Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive1 test
  • Neurodevelopmental disorder with or without seizures and gait abnormalities1 test
  • Neurodevelopmental disorder with or without variable brain abnormalities; NEDBA1 test
  • Neurodevelopmental disorder with poor language and loss of hand skills1 test
  • Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies1 test
  • Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities1 test
  • Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures2 tests
  • Neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies1 test
  • Neurodevelopmental disorder with seizures and brain abnormalities1 test
  • Neurodevelopmental disorder with seizures and brain atrophy1 test
  • Neurodevelopmental disorder with seizures and gingival overgrowth1 test
  • Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements1 test
  • Neurodevelopmental disorder with seizures and speech and walking impairment1 test
  • Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities1 test
  • Neurodevelopmental disorder with severe motor impairment and absent language1 test
  • Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures1 test
  • Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies1 test
  • Neurodevelopmental disorder with spasticity and poor growth1 test
  • Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia1 test
  • Neurodevelopmental disorder with speech impairment and dysmorphic facies1 test
  • Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies1 test
  • Neurodevelopmental disorder with visual defects and brain anomalies1 test
  • Neurodevelopmental disorder, MTOR related1 test
  • Neurodevelopmental, jaw, eye, and digital syndrome1 test
  • Rajab interstitial lung disease with brain calcifications1 test
  • X-linked complex neurodevelopmental disorder1 test

List of services

  • Rett syndrome, DMD del analysis
  • Custom microarray analysis: Order Code: 001
  • Mutation Confirmation: Order Code: 005
  • Whole Exome Sequencing: Order Code: 013
  • Custom Sequence Analysis: Order Code: ExP
  • Whole Genome Sequencing: Order Code: WG_01

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.