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Medical discovery in Utah aided by federal program Michael Paul

Press Releases | 10.19.2016

Lineagen Announces Launch of Proprietary Variant Index to Improve Interpretation of Genetic Basis for...

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Case Studies

High resolution CMA series

Inv dup (15) syndrome

17p12-p11.1 duplication

Angelman syndrome

Chromosome 20p deletion

Mosaic trisomy 21

Turner syndrome

Williams syndrome