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Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder | 345 |
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Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder | 0 | 0 | 14 | 9 | 19 | 14 | 6 |
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CaseReport_Whole Exome Sequencing.pdf | 229 |
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