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Your search keyword '"Brown, Natasha"' showing total 7 results

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7 results on '"Brown, Natasha"'

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1. Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort

2. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome

3. Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

4. A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients

5. A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations

6. Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

7. Inherited variants in CHD3demonstrate variable expressivity in Snijders Blok-Campeau syndrome

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