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Submicroscopic deletion in 7q31 encompassing CADPS2 and TSPAN12 in a child with autism spectrum disorder and PHPV

Nobuhiko Okamoto1, Yoshikazu Hatsukawa, Keiko Shimojima

  • 1Department of Medical Genetics, Osaka Medical Center, Research Institute for Maternal and Child Health, Japan. okamoto@osaka.email.ne.jp

American Journal of Medical Genetics. Part A
|June 1, 2011
PubMed

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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