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42nd and Emile, Omaha, NE 68198 (402) 559-4000 University Computer Use Policy / Copyright Violations- Home
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Shipping & Handling
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Tests Available
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Prenatal Diagnostic Tests
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Cytogenetic Analysis
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Amniotic Fluid Rapid Prenatal Aneuploidy
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Quad Fetal Risk Assessment
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CVS Cytogenetic Analysis
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CVS Interphase FISH
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POC Cytogenetic Analysis
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POC Interphase FISH
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Cytogenetic Analysis
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Adult & Children Diagnostic Tests
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Blood - Cytogenetic Analysis
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Blood - Interphase FISH
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Blood - Metaphase FISH
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Blood - Interphase / Metaphase FISH
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Blood - Breakage Studies
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Blood - Microarray CGH
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Blood - Methylation for Prader-Willi
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Blood - MECP2 Deletion/Duplication
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Blood - MECP2 DNA Sequencing
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Blood - UBE3A Sequencing for Angelman syndrome
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Blood - PTPN11-Tcomp Sequencing
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Blood - PTPN11-Tpart Sequencing
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Blood - PTPN11-Tseg Sequencing
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Biopsy - Cytogenetic Analysis
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Biopsy - Interphase FISH
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Biopsy - Metaphase FISH
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Biopsy - Interphase / Metaphase FISH
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Biopsy - Microarray CGH
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Biopsy - Cell Culture
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Constitutional FISH Panels
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Regions of the Genome Assayed
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Blood - Cytogenetic Analysis
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Cancer Diagnostic Tests
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Hematology / Oncology FISH Panels
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RT-PCR
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HER2/neu - Paraffin Block
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HER2/neu - Solid Tumor Tissue
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UroVysion
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Lymph - Metaphase FISH
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Lymph - Interphase FISH
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Lymph - Cytogenetic Analysis
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Tumor - Metaphase FISH
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Tumor - Interphase FISH
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Tumor - Cytogenetic Analysis
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Bone Marrow - Interphase FISH
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Bone Marrow - Cytogenetic Analysis
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Blood - Interphase FISH
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Blood - Cytogenetic Analysis
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Hematology / Oncology FISH Panels
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Molecular Diagnostic Tests
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PTPN11 for Noonan syndrome
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PTEN
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UBE3A Sequencing
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Methylation Studies
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Fragile X Studies
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DNA Sequencing for Rett syndrome
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PTPN11 for Noonan syndrome
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Prenatal Diagnostic Tests
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Indications for Cytogenetics or FISH Studies
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Genetics Clinics
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Prenatal Diagnosis Options
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Prenatal Diagnosis
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Lab Information
Lab Phone: 402-559-5070
Email: mmihgl@unmc.edu
Supplies: 402-559-5070
Certifications / Licenses:
CLIA # 28D0454363
CAP # 19749-09
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Shipping Address
Cytogenetics Laboratory
Zip 5440
UNMC Shipping & Receiving Dock
668 South 41 Street
Omaha, NE 68105
Newsletter
Postnatal Blood - PTPN11-Tseg Sequencing
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PTPN11-Tseg | |
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Test Includes: |
DNA Sequencing for mutations associated with Noonan syndrome. |
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Indications: |
Suspicion or diagnosis of Noonan syndrome on clinical grounds. Family history of Noonan syndrome. |
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Sample Requirements: |
1-3 ml peripheral blood in an EDTA (purple top) tube. |
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Shipping Requirements: |
Transport at room temperature. Deliver ASAP with a completed Cytogenetics & Molecular Cytogenetics Requisition form. Notify HGL by calling (402) 559-5070 when specimen is being shipped. |
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Turnaround Time: |
21-28 days |
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CPT Code: |
83904(x2), 83896(x2), 83898(x2), 83912, 83894 |