Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole exome sequencing from Central Brazil | PLOS One

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Fig 1 — Fig 1.

Diagram of the testing workflow and number of cases in each step for the genetic diagnosis of ID, GDD and MCA from Central Brazil.
The highlighted rectangles indicate the total of cases for which diagnoses were reached.

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Table 1 — Table 1.

Summary of the molecular results of cases with ID/GDD/MCA investigated with a target gene panel exome sequencing.

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