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Genolife

GTR Lab ID: 506985, Last updated:2024-07-31

Personnel

  • Director: Yenelli Cedano, PhD, ABCC, DABCC, Lab Director
    Phone: México
    Fax: +52-662-4132525
    Email: [email protected]

Conditions and tests

  • 15q11q13 microduplication syndrome1 test
  • 3p- syndrome1 test
  • 5p partial monosomy syndrome1 test
  • 7q11.23 microduplication syndrome1 test
  • Alagille syndrome due to a JAG1 point mutation1 test
  • Alagille syndrome due to a NOTCH2 point mutation1 test
  • Autism, susceptibility to, 31 test
  • Autism, susceptibility to, 51 test
  • Autism, susceptibility to, X-linked 21 test
  • Autism, susceptibility to, X-linked 31 test
  • Bannayan-Riley-Ruvalcaba syndrome1 test
  • Breast cancer, susceptibility to1 test
  • CHARGE syndrome1 test
  • Chromosome 15q13.3 microdeletion syndrome1 test
  • Chromosome 15q25 deletion syndrome1 test
  • Chromosome 16p12.1 deletion syndrome, 520kb1 test
  • Chromosome 16p12.2-p11.2 deletion syndrome1 test
  • Chromosome 16p13.3 duplication syndrome1 test
  • Chromosome 17p13.3 duplication syndrome1 test
  • Chromosome 17P13.3, telomeric, duplication syndrome1 test
  • Chromosome 17q12 deletion syndrome1 test
  • Chromosome 17q21.31 duplication syndrome1 test
  • Chromosome 1p36 deletion syndrome1 test
  • Chromosome 1q21.1 deletion syndrome1 test
  • Chromosome 1q21.1 duplication syndrome1 test
  • Chromosome 22q11.2 deletion syndrome, distal1 test
  • Chromosome 22q11.2 microduplication syndrome2 tests
  • Chromosome 2p16.1-p15 deletion syndrome1 test
  • Chromosome 2q37 deletion syndrome1 test
  • Chromosome 3q29 microdeletion syndrome1 test
  • Chromosome 4Q32.1-q32.2 triplication syndrome1 test
  • Distal 16p11.2 microdeletion syndrome1 test
  • Distal monosomy 10p1 test
  • Miller Dieker syndrome1 test
  • Nance-Horan syndrome1 test
  • Phelan-McDermid syndrome2 tests
  • Prader-Willi syndrome1 test
  • Proximal 16p11.2 microdeletion syndrome1 test
  • Rett syndrome, congenital variant1 test
  • Rubinstein-Taybi syndrome due to 16p13.3 microdeletion1 test
  • Schizophrenia 131 test
  • SIN3A-related intellectual disability syndrome due to a point mutation1 test
  • Smith-Magenis syndrome1 test
  • Waardenburg syndrome type 2E1 test
  • Williams syndrome1 test
  • Y chromosome-related disorders1 test

List of services

  • Custom Deletion/Duplication Testing
  • Prenatal testing
  • Custom Sequence Analysis
  • Custom microarray analysis
  • Identity Testing
  • Whole Exome Sequencing

List of certifications/licenses

Licenses

  • State License, Number: SSP-DGPRS-2012-985, Expiration date: 2029-05-26

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.