Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

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BibTeX:

 {%raw%}@article{celestino2011use,
  title = {Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE},
  author = {Celestino-Soper, Patricia BS and Shaw, Chad A and Sanders, Stephan J and Li, Jian and Murtha, Michael T and Ercan-Sencicek, A Gulhan and Davis, Lea and Thomson, Susanne and Gambin, Tomasz and Chinault, A Craig and others},
  journal = {Human molecular genetics},
  volume = {20},
  number = {22},
  pages = {4360--4370},
  year = {2011},
  publisher = {Oxford University Press},
  public = {yes}
}
{%endraw%}