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Publications by Robert Lyle

Diagnosis by Sequencing: Correction of Misdiagnosis From FSHD2 to LGMD2A by Whole-Exome Analysis

European Journal of Human Genetics
Genetics
2012English

cnvScan: A CNV Screening and Annotation Tool to Improve the Clinical Utility of Computational CNV Prediction From Exome Sequencing Data

BMC Genomics
BiotechnologyGenetics
2016English

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