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CANCER GENETICS AND GENOMICS LABORATORY MYELOID TESTING BC CANCER DEPT. OF PATHOLOGY AND LABORATORY MEDICINE ROOM 3307 600 WEST 10TH AVENUE VANCOUVER BC V5Z4E6ADDRESSOGRAPH OR PATIENT LABEL6048776000
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Step 1: Gather all relevant patient information including medical history, family history, and any previous cancer diagnoses.
02
Step 2: Obtain a consent form signed by the patient to proceed with genetic testing.
03
Step 3: Collect a blood or tissue sample from the patient for genetic analysis.
04
Step 4: Submit the sample to a reputable genetic testing laboratory.
05
Step 5: Wait for the results from the laboratory.
06
Step 6: Review the genetic test results and interpret them in the context of the patient's medical and family history.
07
Step 7: Discuss the findings with the patient and provide appropriate counseling and recommendations based on the results.
08
Step 8: Follow up with the patient to ensure proper understanding of the implications of the genetic test results and to offer ongoing guidance and support.

Who needs cancer genetics and genomics?

01
Individuals with a personal or family history of cancer.
02
Patients with a suspected hereditary cancer syndrome.
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Families with a history of multiple family members affected by cancer.
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Individuals with early-onset or rare types of cancer.
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Patients considering or undergoing cancer treatment who want to assess their risk of developing future cancers.
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People of certain ethnic backgrounds known to have higher rates of specific cancer types.
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Healthcare professionals involved in cancer diagnosis, treatment, and management.
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Researchers studying cancer genetics and genomics.
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Cancer genetics and genomics is the study of how changes in our genes can contribute to the development of cancer.
Medical professionals and researchers are often required to file information on cancer genetics and genomics.
To fill out information on cancer genetics and genomics, one must provide detailed genetic and genomic data related to cancer.
The purpose of cancer genetics and genomics is to better understand the genetic basis of cancer, identify risk factors, and develop targeted treatment options.
Information such as genetic mutations, family history of cancer, and other relevant data must be reported on cancer genetics and genomics.
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