Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder
2019 ◽
Vol 50
(6)
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pp. 2247-2251
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2019 ◽
Vol 58
(3)
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pp. 376-377
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2016 ◽
Vol 26
(6)
◽
pp. 297-301
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2021 ◽
pp. 1-11
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Keyword(s):