Jump to a Specific Test:   Select a Test -- DNA Analysis Tests -- Angelman Syndrome Ashkenazic Jewish Screening Panel 1 Ashkenazic Jewish Screening Panel 2 BCR/ABL Gene Rearrangement (t 9;22) Bloom Syndrome Canavan Disease CFTR Intron 8 Poly (T) Variant Cystic Fibrosis Factor V Leiden Mutation (R506Q) Fanconi Anemia Fragile X Syndrome Fragile X Associated Tremor/Ataxia Syndrome 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) Thrombophilia Panel -- Chromosomal Analysis Tests -- Chromosomal Cancer Analysis Chromosomal Analysis -- FISH Tests -- Angelman Syndrome BCR/ABL Fusion CCND1/IGH CLL Panel Cri du Chat Syndrome DiGeorge/VCFS Syndrome Fetal Aneuploidy Screen Miller-Dieker Syndrome Prader-Willi Syndrome RARA Flanking Probes Smith-Magenis Syndrome Williams Syndrome (Elastin) > Overview > DNA Analysis > Chromosomal Analysis > FISH > Parentage   FISH ANALYSIS: Bcr/Abl Gene Rearrangement (t 9;22)   Please contact the Cytogenetic Laboratory for information.   Forms and Transport & Shipping Informtaion > Medical Genetics Test Requisition Form > Medical Genetics Specimen Transport and Shipping Information

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