Precise molecular diagnoses in clinical exome cases
Weimin Bi and colleagues apply copy number variant and runs of homozygosity detection.
viernes, 14 de junio de 2019
Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases | Genome Medicine | Full Text
Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases | Genome Medicine | Full Text
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