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Okur‐Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.

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Title: Okur‐Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.
Authors: Chiu, A. T. G.1,2, Pei, S. L. C.1, Mak, C. C. Y.1, Leung, G. K. C.1, Yu, M. H. C.1, Lee, S. L.1,2, Vreeburg, M.3, Pfundt, R.4, Van Der Burgt, I.4, Kleefstra, T.4,5, Frederic, T.M.‐t.6,7,8, Nambot, S.6,7, Faivre, L.6, Bruel, A.‐l.8, Rossi, M.9,10, Isidor, B.11,12, Küry, S.11, Cogne, B.11, Besnard, T.11, Willems, M.13
Source: Clinical Genetics. Apr2018, Vol. 93 Issue 4, p880-890. 12p. 1 Color Photograph, 3 Diagrams, 7 Charts.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Apr2018, Vol. 93 Issue 4, p880-890. 12p. 1 Color Photograph, 3 Diagrams, 7 Charts.
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