Ear, Nose and Throat. Enhanced clinical utility, maximized diagnostic yield. Our clinical WES is now equipped with a 99. Ear, Nose and Throat. Easy ordering and networking platform for clinicians. Published on March 16, 2018.

We offer comprehensive genetic diagnostics for a number of disorders associated with hereditary cancer susceptibility. These cancer panels cover genes associated with cancer types originating from the gastrointestinal tract, the endocrine and neuroendocrine systems, different organs such as the lungs, kidneys, liver, pancreas, skin, and eyes, gathering the known genetic defects presenting early in childhood.

Blueprint Genetics wants to change the field of cardiogenetics by providing our customers the most rapid and comprehensive diagnostics and clinical interpretation available. Blueprint Genetics diagnostic panels cover majority of genes associated with cardiomyopathies, arrhythmias and vascular diseases. Find a test for your patient. 22 diagnostic tests, covering 242 genes.

Genetic diagnostics is the most efficient way to subtype hereditary dermatological diseases, providing the necessary information to make confident individualized treatment and management decisions. Moreover, detection of the causative mutation establishes the mode of inheritance within the family, which is essential for well-informed genetic counseling. Find a test for your patient. 14 diagnostic tests, covering 156 genes.

Many endocrine disorders may present as part of a syndrome with multiple manifestations. Accurate molecular diagnosis is therefore important for optimizing treatment, and in identifying other manifestations of the syndrome for which the patient should be screened. Find a test for your patient. We use our own proprie.

Find a test for your patient. 7 diagnostic tests, covering 82 genes. Genetic diagnosis is also c.

Accurate genetic diagnosis is necessary to confirm the diagnosis of certain hematological malignancies and to find the optimal treatment for affected patients. Establishing the underlying genetic defect and inheritance pattern further allows family member testing to identify at-risk relatives. Find a test for your patient. 16 diagnostic tests, covering 176 genes.

Accurate genetic diagnosis of the immunodeficiency, combined with a detailed disease phenotype, is crucial in characterizing these rare diseases. It also improves treatment and follow-up strategies for affected patients and their family members. From sample to clinical interpretation. We sequence the DNA in our lab with our proprietary targeted sequencing method OS-Seq , developed at Stanford.

Genetic diagnostics is the most efficient way to subtype malformations, providing the necessary information to make confident individualized treatment and management decisions. Moreover, identifying the causative mutation establishes the mode of inheritance within the family, which is essential for well-informed genetic counseling. Find a test for your patient. 32 diagnostic tests, covering 442 genes.

Genetic diagnostics is the most efficient way to subtype metabolic disorders, providing the necessary information to make confident individualized treatment and management decisions. For example, in coenzyme Q10 deficiency, a correct diagnosis is important because some patients may show a favorable response to CoQ10 treatment. Find the test for your patient. 22 diagnostic tests, covering 354 genes.