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COSMID: A Web-based Tool for Identifying and Validating CRISPR/Cas Off-target Sites
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Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing
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Clinical Utility of Array Comparative Genomic Hybridization: Uncovering Tumor Susceptibility in Individuals with Developmental Delay
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Genomic Characterization of Prenatally Detected Chromosomal Structural Abnormalities Using Oligonucleotide Array Comparative Genomic Hybridization
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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes
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Prostate cancer genes associated with TMPRSS2-ERG gene fusion and prognostic of biochemical recurrence in multiple cohorts
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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
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Martin, Christa
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Adam, MP
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Bao, Gang
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Barwick, BG
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Blum, Werner F.
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Bouzyk, M
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Child, Christopher J.
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American Journal of Medical Genetics Part A
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