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t(3;9)(q11-12;q22)

MedGen UID:: 318464
•Concept ID:: C1711152
•: Cell or Molecular Dysfunction

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(3;9)(q11-12;q22)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosomal translocation
      - t(3;9)(q11-12;q22)

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t(3;9)(q11-12;q22)
t(3;9)(q11-12;q22)

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