The emerging genetic landscape of cerebral palsy
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Elsevier
Reference87 articles.
1. An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome;Abdollahpour;Eur J Hum Genet,2015
2. Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature;Abou Jamra;Am J Hum Genet,2011
3. Predicting functional effect of human missense mutations using PolyPhen-2;Adzhubei;Curr Protoc Hum Genet,2013
4. Continuous cardiotocography (CTG) as a form of electronic fetal monitoring (EFM) for fetal assessment during labour;Alfirevic;Cochrane Database Syst Rev,2013
5. De novo mutations in epileptic encephalopathies;Allen;Nature,2013
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