dmcn12425-sup-0001-FigS1.docWord document74KFigure S1: Microcephaly questionnaire. Comprehensive medical and family history and detailed clinical examination data can be summarized in a standard questionnaire. CMV, cytomegalovirus; IUGR, in utero growth retardation; OFC, occipitofrontal head circumference; ENT, ears, nose, and throat.
dmcn12425-sup-0002-FigS2.docWord document85KFigure S2: Diagnostic work-up form for microcephaly. Diagnostic work-up results of patients with microcephaly can be summarized in a standard form. MRI, magnetic resonance imaging; CT, computed tomography; CGH-array, comparative genomic hybridization array; FISH, fluorescence in situ hybridization; MLPA, multiplex ligation-dependent probe amplification; qPCR, quantitative real-time PCR; CSF, cerebrospinal fluid; DBS, dried blood spots; electrophor, electrophoresis.

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