Correction: Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases.

[This corrects the article DOI: 10.1371/journal.pone.0133636.].

S3, S4 and S5 Tables appear incorrectly in the published article. Please see the correct tables below.

The list of 561 Mendelian diseases.

(XLSX)

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Results of normalization analysis of three patients (P88, P89 and P90).

We detected a microduplication of chromosome 10 in patient P88, the gender ratio was about 1.42. We detected a microduplication of chromosome 9 in patient P89, the gender ratio was about 1.31. We detected a microdeletion in chromosome 17 (16773072–20222149) in patient P90, the gender ration was about 0.55.

(DOC)

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Primer pairs designed for validation of mutations by Sanger sequencing or real-time PCR.

(DOC)

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