Showing 1 - 2 results of 2 for search 'Smrithi Salian', query time: 0.01s Refine Results
  1. 1
    Novel ALOX12B mutation identified in parents following single nucleotide polymorphism microarray testing of banked DNA from a fatal case of congenital ichthyosis

    Novel ALOX12B mutation identified in parents following single nucleotide polymorphism microarray testing of banked DNA from a fatal case of congenital ichthyosis by Smrithi Salian, Ashish Gupta, Anju Shukla, Katta M Girisha

    Published 2016
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    Focal dermal hypoplasia with a de novo mutation p.e300FNx01 of porcn gene in a male infant

    Focal dermal hypoplasia with a de novo mutation p.e300FNx01 of porcn gene in a male infant by Swathi Sunil Rao, Rathika D Shenoy, Smrithi Salian, Katta M Girisha

    Published 2016
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: