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Updated: Aug 9, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5
1Cytogenetics Unit, Prince of Wales Hospital, Sydney, Australia.
This study details a rare interstitial deletion 15q genetic disorder in a young boy. Key features include distinct facial anomalies and developmental delays, highlighting the syndrome's impact.
Area of Science:
- Genetics
- Pediatrics
- Human Malformations
Background:
- Interstitial deletion 15q is a rare chromosomal abnormality.
- Genetic rearrangements can lead to complex phenotypes in children.
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