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Patients initialsDate of the brightest order.(MM/DD/YYY)Complete this form faster and more easily on www.centoportal.comFOR CANTONESE USE ONLY DO NOT COVER Priority (optional) FAST processing×Prenatal
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To fill out for centogene use only, follow these steps:
02
Obtain the form from centogene.
03
Read the instructions carefully before starting to fill out the form.
04
Fill out the required personal information accurately, such as name, contact details, and identification number.
05
Provide the necessary medical information requested by centogene.
06
Ensure all sections of the form are properly completed, including any additional information or documentation required.
07
Double-check the form for any errors or missing information before submitting it.
08
Once completed, submit the form to centogene through the designated method (online, email, or in person).
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If applicable, make sure to include any additional supporting documents or reports required by centogene.
10
Keep a copy of the filled-out form and any submitted documents for your records.

Who needs for centogene use only?

01
Those who need for centogene use only are individuals or entities who require the specific services or information provided by centogene.
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This can include healthcare professionals, researchers, patients, or organizations that have a valid reason to access the resources, testing, or expertise offered by centogene.
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It is important to note that centogene may have specific criteria or eligibility requirements for individuals or entities to be eligible for their services for centogene use only.
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It refers to specific documents or information that are designated for processing and assessment by Centogene, a genetic testing company.
Individuals or entities seeking genetic testing and analysis through Centogene are required to file these documents.
Filling out for Centogene use only involves completing the designated forms accurately with the required personal and medical information, and submitting them according to the provided instructions.
The purpose is to gather genetic information necessary for testing, diagnosis, and research related to genetic conditions and diseases.
Key information includes patient identification details, medical history, family history, and any relevant test results.
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