Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5

M Y Yip1, M Selikowitz, N Don

  • 1Cytogenetics Unit, Prince of Wales Hospital, Sydney, Australia.

Summary

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.

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