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Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.

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Title: Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.
Authors: Yoon, Jihoon G.1,2 (AUTHOR), Jang, Hyunsoo3,4 (AUTHOR), Lee, Seungbok1,5 (AUTHOR), Jang, Se Song5 (AUTHOR), Park, Soojin5 (AUTHOR), Cho, Jaeso1,5,6 (AUTHOR), Kim, Minji3,4 (AUTHOR), Han, Jiye3,4 (AUTHOR), Yun, Hyounji3,4 (AUTHOR), Kim, Man Jin1 (AUTHOR), Kim, Soo Yeon1,5 (AUTHOR), Kim, Woo Joong5 (AUTHOR), Cho, Anna6 (AUTHOR), Lee, Jin Sook7 (AUTHOR), Choi, Murim8 (AUTHOR), Fernandez-Jaen, Alberto9 (AUTHOR), Silva, Sebastian10,11 (AUTHOR), Uribe-San-Martín, Reinaldo12,13 (AUTHOR), Cantillano, Christian13,14 (AUTHOR), Miyake, Noriko15 (AUTHOR)
Source: Genome Medicine. 8/6/2025, Vol. 17 Issue 1, p1-20. 20p.
Database: Academic Search Ultimate
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  Data: Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.
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  Data: <searchLink fieldCode="JN" term="%22Genome+Medicine%22">Genome Medicine</searchLink>. 8/6/2025, Vol. 17 Issue 1, p1-20. 20p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=187165692
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