Search Results - Smrithi Salian

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    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
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    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
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