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Array-CGH / Cytogenetics 


Array Comparative Genomic Hybridisation (Array-CGH) is currently the principal test for the detection of genomic imbalances: it has replaced karyotyping as the front-line test for neonatal, paediatric and adult patients with neurodevelopmental disorders and dysmorphism or multiple congenital anomalies, and for the detection of pathogenic genomic imbalances at prenatal diagnosis or in fetal losses.


Ms Emma-Jane Cassidy
Tel. 01722 429077

For full details of our array-CGH service see:


Chromosome analysis (Karyotyping)

Traditional chromosome analysis (karyotyping) is provided for certain referral categories such as testing for balanced chromosome rearrangements.

Page Last Updated: 26/02/2019 11:54 
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