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single gene disorders
How are Single Gene Disorders Diagnosed?
Diagnosis often involves
genetic testing
methods such as
polymerase chain reaction (PCR)
,
sequencing
, and
chromosomal microarray
. These tests identify mutations in specific genes. Family history and clinical presentation are also critical in the diagnostic process.
Frequently asked queries:
What are Single Gene Disorders?
Why Study Single Gene Disorders in Epidemiology?
How are Single Gene Disorders Diagnosed?
What are the Challenges in Managing Single Gene Disorders?
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