Constitutional Test Menu

801 Chromosome Analysis, Blood
803 Chromosome Analysis, Blood, Abridged (Examination for Familial Chromosome Rearrangements)
850 Chromosome Analysis, Amniotic Fluid
852 Chromosome Analysis, Amniotic Fluid, Abridged (must also order 890)
855 Chromosome Analysis, Chorionic Villus Sample
857 Chromosome Analysis, CVS, Abridged (must also order 890)
831 Chromosome Analysis, Products of Conception/ Tissue Biopsy
860 Tissue culture and shipment for additional testing

828 Molecular Analysis, Fragile-X, Genetic Diagnosis
889 Methylation-Specific PCR, SNRPN gene, 15q11.2
890 Chromosomal Microarray Analysis (CMA), SNP-based
- Phenotype form – MicroArray postnatal
890FAM Microarray Targeted Analysis (Family Studies)
895M47 PlainSEEK Panel (Coming soon)
895M64 Exome Sequencing- Proband Analysis Only
- Exome Sequencing Forms
895M65 Exome Sequencing- Duo Analysis
895M66 Exome Sequencing- Trio Analysis
895M68 Sudden Unexplained Death in the Young (SUDY) Exome
895M50 Targeted Variant Analysis via Sanger DNA Sequencing
- See Inherited Diseases – Sequence Variant Testing

873 Pre-natal Aneuploidy Panel, Amniotic Fluid
875 Stillbirth Aneuploidy Panel, Paraffin Embedded
871F28 DiGeorge /Velo-cardio-facial/Schpritzen/Conotruncal anomaly Syndrome, Deletion 22q11.2, TUPLE1
871F34 SRY (Sex determining Region of Y), Yp11.3
870F52 X and Y sex chromosomes

UW Cytogenetic Services and Molecular Genetics 465 Henry Mall, Room 419 Madison, WI 53706

cytogenetics@mail.slh.wisc.edu Phone: 608-262-0402 / 800-862-1013 Fax: 608-265-7818