Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.

  • Aayush Gupta, Yugal Sharma, Kirti Deo, Shamsudheen Vellarikkal, Rijith Jayarajan, Vishal Dixit, Ankit Verma, Vinod Scaria, Sridhar Sivasubbu
  • F1000Research, July 2015, Faculty of 1000, Ltd.
  • DOI: 10.12688/f1000research.6779.1

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http://dx.doi.org/10.12688/f1000research.6779.1

The following have contributed to this page: Dr Aayush Gupta, Vinod Scaria, and Yugal Sharma