A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH

Genetic Counseling (Geneva, Switzerland)
|March 26, 2015
PubMed
Summary

This study details a patient with developmental delay and unique physical features, identifying a 7p chromosomal abnormality. The findings link specific genetic duplications and deletions on chromosome 7 to observed neurodevelopmental and congenital conditions.

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