All Oncology Tests

Acute Lymphocytic Leukemia (ALL) Panel

Acute Lymphocytic Leukemia (ALL) Panel

Acute Myelocytic Leukemia (AML) : NPM1 codon 12 Variants

Acute Myelocytic Leukemia (AML) : NPM1 codon 12 Variants

Acute Myelocytic Leukemia (AML) Panel

Acute Myelocytic Leukemia (AML) Panel

Acute Promyelocytic Leukemia (APL) FISH Analysis

Acute Promyelocytic Leukemia (APL) FISH Analysis

Brain Tumor : 1p/19q Co-Deletion Analysis

Brain Tumor : 1p/19q Co-Deletion Analysis

Brain Tumor : CDKN2A/B Deletion Analysis

Brain Tumor : CDKN2A/B Deletion Analysis

Brain Tumor : EGFR Amplification Analysis

Brain Tumor : EGFR Amplification Analysis

Brain Tumor : IDH1 R132H Variant Analysis

Brain Tumor : IDH1 R132H Variant Analysis

Brain Tumor : NEK1 Deletion Analysis

Brain Tumor : NEK1 Deletion Analysis

Brain Tumor : NF1 Deletion Analysis

Brain Tumor : NF1 Deletion Analysis

Brain Tumor : PTEN Deletion Analysis

Brain Tumor : PTEN Deletion Analysis

Brain Tumor : TP53 Deletion Analysis

Brain Tumor : TP53 Deletion Analysis

Chromosome Analysis (bone marrow, lymph nodes, stim/umstim blood)

Chromosome Analysis (bone marrow, lymph nodes, stim/umstim blood)

Chronic Lymphocytic Leukemia (CLL) Panel

Chronic Lymphocytic Leukemia (CLL) Panel

Colorectal Cancer : KRAS Variant Analysis

Colorectal Cancer : KRAS Variant Analysis

Colorectal Cancer : NRAS Variant Analysis

Colorectal Cancer : NRAS Variant Analysis

Lung Adenocarcinoma : BRAF Mutation analysis (V600E)

Lung Adenocarcinoma : BRAF Mutation analysis (V600E)

Lung Adenocarcinoma : EGFR Amplification and Mutation Analysis

Lung Adenocarcinoma : EGFR Amplification and Mutation Analysis

Lung Adenocarcinoma : EGFR Mutation Analysis

Lung Adenocarcinoma : EGFR Mutation Analysis

Lung Adenocarcinoma : PTEN Mutation Analysis

Lung Adenocarcinoma : PTEN Mutation Analysis

Melanoma : BRAF Mutation Analysis (V600E & V600K)

Melanoma : BRAF Mutation Analysis (V600E & V600K)

Pediatric Acute Lymphoblastic Leukemia (P-ALL) Panel

Pediatric Acute Lymphoblastic Leukemia (P-ALL) Panel

Meet Makayla Gunn

Meet Makayla Gunn

Makayla was diagnosed with Rett Syndrome in April of 2015 at the age of two.   At about 18 months, we noticed she had started some repetitive hand motions, and her pediatrician was a little concerned that she did not have many words.  She had learned some sign language, and was saying ‘mama’ and ‘dada’, but that was it.  Then she suddenly stopped all of that.  At her 2 year old check-up, the pediatrician referred us to BabyNet, ...

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