Associated Papers
Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.
Raizis AM et al.
The New Zealand Medical Journal, 2009
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects.
Gong W et al.
Journal of Medical Genetics, 2001
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Lam CW et al.
Journal of Medical Genetics, 2000
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