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Home / Specialties & Programs / Genetic Services / Tests / DNA Analysis
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Medical Genetics
  • About Us
  • Genetic Counseling
  • Cytogenetics Laboratory
  • Molecular Genetics Laboratory
  • Parentage Testing
  • Where to Send Specimens
  • Tests
    • Angelman Syndrome
    • Angelman Syndrome (FISH Analysis)
    • Ashkenazi Jewish Genetic Screening - Panel 1
    • Ashkenazi Jewish Genetic Screening - Panel 2
    • Bcr/Abl Gene Rearrangement , Quantitative Assay
    • BCR-ABL Gene Rearrangement
    • Bloom Syndrome
    • Canavan Disease Carrier Testing
    • Cancer Chromosomal Analysis
    • CFTR Intron 8 Poly(T) Variant
    • Chromosomal Analysis
    • Chromosomal Analysis Testing
    • Cri du Chat Syndrome
    • Cystic Fibrosis
    • DiGeorge/VCFS Syndrome
    • DNA Analysis
    • Factor V Leiden Mutation
    • Familial Dysautonomia Carrier Testing
    • Fanconi Anemia Group C Carrier Testing
    • Fetal Aneuploidy
    • FISH
    • Fragile X Tremor Ataxia
    • Gaucher Disease Carrier Testing
    • Glycogen Storage Disease Type 1A Carrier Testing
    • Huntington Disease
    • Janus Kinase Mutation
    • Miller-Dieker Syndrome
    • MTHFR Variant
    • Mucolipdosis IV Carrier Testing
    • Niemann Pick Disease Carrier Testing
    • Prader Willi Syndrome Testing
    • Prader-Willi Syndrome (FISH Analysis)
    • Prothrombin Mutation
    • Smith-Magenis Syndrome
    • STS/Kallman Syndrome
    • Tay-Sachs Disease Carrier
    • Tay-Sachs Disease Carrier Testing (Hexosaminidase A )
    • Thrombophilia Panel
    • Williams Syndrome (Elastin)
 

DNA Analysis

The Molecular Genetics Laboratory is currently offering testing for the following disorders.   All specimens submitted for analysis should be accompanied by the UCSD Medical Genetics Test Requisition Form.

Tests Offered

  • Angelman Syndrome
  • Ashkenazi Jewish Screening Panel 1
  • Ashkenazi Jewish Screening Panel 2
  • BCR/ABL, t 9;22 (Qualitative)
  • BCR/ABL, t 9;22 (Quantitative)
  • Bloom Syndrome
  • Canavan Disease
  • CFTR Intron 8 Poly (T) Variant
  • Cystic Fibrosis
  • Factor V Leiden Mutation (R506Q)
  • Familial Dysautonomia
  • Fanconi Anemia Group C
  • Fragile X Associated Tremor/Ataxia Syndrome , Premature Ovarian Failure
  • Gaucher Disease
  • Glycogen Storage Disease Type 1A
  • Huntington Disease
  • JAK2 Mutation (V617F)
  • MTHFR Variant (C677T)
  • Mucolipidosis Type IV
  • Niemann-Pick Disease
  • Prader-Willi Syndrome
  • Prothrombin-Factor II Gene Mutation (G20210A)
  • RhD Genotyping (Fetal)
  • Tay-Sachs Disease
  • Tay-Sachs Disease (Biochemical Analysis)
  • Thrombophilia Panel

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