Welcome to the Molecular Cytogenetics Laboratory at
SSM Cardinal Glennon Children's Medical Center.
Medicare Provider #: 26-3300
CAP #: 19214-01
CLIA #: 26D0045275
Cytogenetic Testing:
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Molecular Testing:
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Postnatal - Stat Blood
Chromosomes
- Routine Blood
Chromosomes
- High Resolution
- Fragile-X
- Induced breakage study
(ex: Fanconi Anemia,
Ataxia telangectasia)
- Skin biopsy
- Products of Conception |
Microdeletion
Syndromes - Williams Syndrome
- Prader-Willi Syndrome
- Angleman Syndrome
- Miller-Dieker Syndrome
- Smith-Magenis Syndrome
- Di George Syndrome,
Velo-cardiofacial Syndrome
- Wolf-Hirschhorn Syndrome
- Other syndromes,
FISH arranged upon request |
Prenatal - Amniotic Fluid
- Chorionic Villus Sampling
- Fetal Cord Blood |
Cancer Specific - CML: ABL-BCR
t(9;22)(q34;q11.2)
- AML-M3: PML-RARA
t(15;17)(q22;q11-q21)
- MLL (11) (q23) |
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Cancer - Bone Marrow
- Oncology Blood
- Solid Tumor
- Lymph Node
- Pleural Effusion
- Core Biopsy |
Aneuploidy - Prenatal specimen to rule
out common aneuploidy
(18), (13), (21), X and Y
- Postnatal specimen to rule out
any aneuploid chromosome
- Cancer specimen to rule out
any aneuploid chromosome |
Miscellaneous - Set Up EB
Transformed
Cell Line
- Cell Line
Chromosome
Analysis |
Unidentified
Rearrangements
Or Marker - Painting probe for any
chromosome |
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Direct - Fragile-X DNA:
FRAXA & FRAXE |
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Molecular Testing - Prader-Willi/Angelman
Uniparental Disomy
- Several cancer rearrangements
upon request |