Unravelling the genetic causes of syndromic Intellectual Disability in the era of exome sequencing

Références BibTex

@InProceedings{ZOCRBAJDSVASCC12,
  author       = {Zara, I. and Oppo, M. and Chiappe, F. and Reinier, F. and Berutti, R. and Atzeni, R. and Jones, C. and Dessì, V. and Serra, G. and Valentini, M. and Angius, A. and Sanna, S. and Cucca, F. and Crisponi, L.},
  title        = {Unravelling the genetic causes of syndromic Intellectual Disability in the era of exome sequencing},
  booktitle    = {ESHG (European Society of Human Genetics) 2012, Nuremberg, Germany},
  month        = {june},
  year         = {2012},
  keywords     = {Exome Sequancing, Rare disease, Intellectual Disability, Rare variants},
  url          = {https://publications.crs4.it/pubdocs/2012/ZOCRBAJDSVASCC12},
}

Autres publications dans la base