Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features

@article{Bertok2015ClinicalAM,
  title={Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features},
  author={S. Bertok and Mojca Žerjav Tan{\vs}ek and P. Kotnik and T. Battelino and M. Volk and V. Pecile and L. Cleva and P. Gasparini and J. Kova{\vc} and T. Hovnik},
  journal={Slovenian Journal of Public Health},
  year={2015},
  volume={54},
  pages={69 - 73}
}
Abstract Introduction. Developmental delay and dysmorphic features affect 1 - 3 % of paediatric population. In the last few years molecular cytogenetic high resolution techniques (comparative genomic hybridization arrays and single-nucleotide polymorphism arrays) have been proven to be a first-tier choice for clinical diagnostics of developmental delay and dysmorphic features. Methods and results. In the present article we describe the clinical advantages of molecular cytogenetic approach… Expand

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