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Constitutional Cytogenetics Requisition (noncancer) ACCOUNT INFORMATION 5323 Harry Hines Blvd U5.100 Dallas, Texas 75390 PHONE: 2146457057 Toll Free: 8778878136 FAX: 2146457035 CIA #45D0659587, CAP
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How to fill out constitutional cytogenetics requisition non-cancer

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How to fill out constitutional cytogenetics requisition non-cancer:

01
Start by providing your personal information such as your full name, date of birth, and contact information. This will help in identifying the patient accurately.
02
Indicate the reason for the test and explain the medical history or any relevant clinical findings that led to the need for the cytogenetics test.
03
Specify the type of sample to be tested, whether it is blood, bone marrow, or any other type of specimen.
04
Provide detailed information about the referring physician, including their name, contact information, and any additional information that may be useful for the laboratory to make contact if needed.
05
Include relevant insurance details, such as the patient's insurance provider and policy number, if applicable.
06
Indicate any specific requirements or instructions for the laboratory, such as the need for rush processing or specific tests to be performed.
07
Sign and date the requisition form to acknowledge your consent and agreement to proceed with the cytogenetics test.

Who needs constitutional cytogenetics requisition non-cancer?

01
Individuals who have been referred by their physicians for genetic testing to understand any underlying chromosomal abnormalities or genetic conditions.
02
Patients who are experiencing unexplained developmental delays, intellectual disabilities, or birth defects that may have a genetic basis.
03
Couples who are planning to have children or are undergoing fertility treatments and wish to assess their risk of passing on certain genetic disorders to their offspring.
04
Individuals with a family history of genetic conditions or chromosomal abnormalities, who want to understand their own risk or make informed reproductive decisions.
05
Patients who have previously been diagnosed with a genetic condition and require further testing to monitor their condition or assess the risk of recurrence in their offspring.
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