Associated Papers
Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss.
Sheppard S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
29907799 (PubMed )
Supplement: 41436_2018_4_MOESM3_ESM.xlsx › variant-_capture___coverage
A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.
Yu X et al.
Neuroscience Bulletin, 2018
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Marcelis CL et al.
Human Mutation, 2008
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