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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 5 of 5 1 The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Kortüm, Fanny; Das, Soma; Flindt, Max... In: ISSN: 0022-2593 ; EISSN: 1468-6244 ; Journal of Medical Genetics ; https://hal.archives-ouvertes.fr/hal-00616882 ; Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (6), pp.396. ⟨10.1136/jmg.2010.087528⟩ (2011) BASE Show details 2 The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Kortüm, Fanny; Das, Soma; Flindt, Max. - : British Medical Journal Publishing Group, 2011 BASE Show details 3 The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Kortüm, Fanny; Das, Soma; Flindt, Max. - : British Medical Journal Publishing Group, 2011 BASE Show details 4 The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Kortüm, Fanny; Das, Soma; Flindt, Max. - 2011 BASE Show details 5 The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Kortüm, Fanny; Das, Soma; Flindt, Max. - : BMJ Publishing Group, 2011 BASE Show details

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