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genomic imbalances
How are Genomic Imbalances Detected?
Detection of genomic imbalances involves several techniques. The most commonly used methods include
karyotyping
,
fluorescence in situ hybridization (FISH)
, and
chromosomal microarray analysis (CMA)
. More recently,
next-generation sequencing (NGS)
has also been employed to identify these imbalances with higher resolution and accuracy.
Frequently asked queries:
What are Genomic Imbalances?
How are Genomic Imbalances Detected?
What Conditions are Associated with Genomic Imbalances?
How Do Genomic Imbalances Affect Development?
What is Emotional and Psychological Well-being in Pediatrics?
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When is EFM Indicated?
How Do Coding and Billing Impact Reimbursement?
What Is the Future of Administrative Costs in Pediatrics?
What Are the Next Steps If Hearing Loss is Confirmed?
What Are the Changes in the Immune System?
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