Michael Lyons to High-Throughput Nucleotide Sequencing
This is a "connection" page, showing publications Michael Lyons has written about High-Throughput Nucleotide Sequencing.
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Smith JA, Holden KR, Friez MJ, Jones JR, Lyons MJ. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318.
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