Pathology

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A
07/20/2018 Alpha Globin Gene Analysis (Sequencing and Del/Dup)
03/13/2014 Autopsy and Death Procedures
B
02/15/2023 BCR-abl by PCR, Qualitative, Blood/Bone Marrow (Mayo)
04/24/2023 BCR-abl, p190, Quant Monitor (Mayo)
04/24/2023 BCR-abl, p210, RNA Quant, Monitor CML (Mayo)
03/16/2023 BCR-abl, Tyrosine Kinase Inhibitor Resistance, Kinase Domain Mutation Screen
08/02/2015 Beckwith-Wiedemann Syndrome & Russell-Silver Syndrome Methylation, Blood
03/13/2014 Bronchoalveolar Lavage Cell Count and Differential
C
08/02/2015 CFTR 106 Mutation Panel Sequencing
07/20/2018 CFTR Known Mutation
09/05/2023 CGH for Oncology
03/13/2023 CGH with SNP Array
08/30/2023 CGH with SNP Array and Limited GBand
04/20/2023 Chromosome, Blood, Breakage Syndromes
04/20/2023 Chromosome, Blood, Limited G-Band
04/20/2023 Chromosome, Blood, Newborn Less Than 21 Days
03/13/2023 Chromosome, Blood, Sex Chromosome Study
10/08/2015 Chromosome, Skin/POC (Fairview)
04/20/2023 Chromosomes, Blood, High Resolution (Fairview University)
09/05/2023 Chromosomes, Bone Marrow
07/20/2023 Chromosomes, Leukemic Blood (Fairview)
09/05/2023 Chromosomes, Malignant Tissue (Fairview University)
03/13/2014 Cilia Biopsy
09/05/2023 Comparative Genomic Hybridization (CGH) with Limited High Resolution G-Bands
12/19/2023 Comprehensive Epilepsy Panel
01/16/2024 CONSTITUTIONAL CHROMOSOMAL MICROARRAY (COPY NUMBER)
01/12/2024 CONSTITUTIONAL LIMITED CHROMOSOMAL MICROARRAY (COPY NUMBER ONLY, CHARGED)
01/12/2024 CONSTITUTIONAL LIMITED CHROMOSOMAL MICROARRAY FOR PARENTAL FOLLOW UP (COPY NUMBER ONLY, NO CHARGE)
01/22/2018 Copper Liver, Tissue
06/19/2018 Craniodysmorphology (FGFR) Full Panel with TWIST Sequencing
03/07/2024 CYP21A2 (CAH) Evaluation Sequencing
02/05/2013 CYP21A2 (CAH) Known Sequencing
11/03/2017 Cytochrome P450 2C19 Sequencing
11/03/2017 Cytochrome P450 2C9 Sequencing
03/13/2014 Cytology, Herpes
03/13/2014 Cytology, Urine
03/13/2014 Cytology, Washings
D
06/17/2021 Disaccharidase on GI Biopsies
04/18/2018 DNA Marker Pre BMT Engraftment
E
09/15/2017 Electron Microscopy (Mayo)
03/13/2014 Electron Microscopy, Tissue (HCMC)
09/07/2023 Electron Microscopy, Whole Blood
04/25/2016 Expanded RASopathy Panel (14 Genes)
F
12/28/2023 Fanconi Anemia
11/12/2014 Fatty Acid Oxidation Probe, Fibroblasts
09/21/2022 Fibroblast Culture for Biochemical or Molecular Testing
01/24/2018 Fibroblast Culture, Tissue
01/12/2024 FISH Interphase
08/30/2023 FISH Locus Specific (Metaphase)
09/08/2023 FLT3
08/02/2015 Fragile X Molecular Analysis (Mayo)
10/31/2018 Frozen Sections - Indications for Intraoperative Consultations
G
03/30/2020 GAA Enzyme Activity
11/18/2016 Galactosemia Gene Analysis 14 Panel
02/19/2021 GALT Full Gene Analysis
H
08/02/2015 Hemochromatosis (HFE) Sequencing
I
01/28/2019 Inherited Thrombocytopenia Panel
02/12/2013 Iron, Liver Tissue
K
02/12/2013 Kidney Biopsy, Routine Surgical Pathology
L
08/14/2013 Lactase on GI Biopsies
M
12/07/2023 MTHFR Genotype
08/11/2016 Muscle Biopsy
02/07/2013 Myotonic Dystrophy
N
01/22/2018 Nerve Biopsy
12/19/2023 Neurofibromatosis Type 1 (NF1) Known Mutation
12/19/2023 Neurofibromatosis Type 1 (NF1) Sequencing
12/19/2023 Neurofibromatosis Type1-Like (SPRED1) Known Mutation
12/19/2023 Neurofibromatosis Type2 (NF2) Known Mutation
12/19/2023 Neurofibromatosis Type2 (NF2) Sequencing & Deletion/Duplication
12/19/2023 NF1 Sequencing & Deletion/Duplication
O
08/17/2022 OneOme RightMed Pharmacogenetics
P
11/15/2023 Pap Thin Prep
10/05/2022 Pharmacoscan Panel
04/06/2018 PHOX2B Full Gene Sequence
12/02/2022 Platelet Transmission Electron Microscopy
01/22/2018 Postmortem Screening
08/02/2015 Prader-Willi/Angelman Syndrome Molecular Analysis Methylation
08/17/2022 Primary Ciliary Dyskinesia Panel
R
10/02/2014 Rett Syndrome (MECP2) Sequencing
S
03/07/2018 Sotos Syndrome (NSD1) Deletion/Duplication
03/07/2018 Sotos Syndrome (NSD1) Sequencing
01/22/2018 Surgical Pathology Consultation
T
02/11/2020 Target B-ALL Fusion Analysis
04/25/2023 Targeted Oncology Microarray, Wilms Tumor or Neuroblastoma
12/19/2023 TPMT/NUDT15/CEP72 Panel
12/19/2023 Tuberous Sclerosis (TSC1/TSC2) Complex Sequencing & Deletion/Duplication
U
03/07/2018 Uniparental Disomy Chromosome 6