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
|