Investigating the child with intellectual disability
Author:
Affiliation:
1. Murdoch Children's Research Institute; Royal Children's Hospital; Melbourne Victoria Australia
2. Department of Paediatrics; University of Melbourne; Melbourne Victoria Australia
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jpc.14202/fullpdf
Reference26 articles.
1. Genetic studies in intellectual disability and related disorders;Vissers;Nat. Rev. Genet.,2016
2. Comprehensive evaluation of the child with intellectual disability or global developmental delays;Moeschler;Pediatrics,2014
3. Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules;Kochinke;Am. J. Hum. Genet.,2016
4. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA;Coffee;Am. J. Hum. Genet.,2009
5. Epigenetics of fragile X syndrome and fragile X-related disorders;Kraan;Dev. Med. Child Neurol.,2018
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