Showing 1 - 2 results of 2 for search 'Shubham Basu', query time: 0.02s Refine Results
  1. 1
    A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease.

    A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease. by Gavin R Oliver, Xiaojia Tang, Laura E Schultz-Rogers, Noemi Vidal-Folch, W Garrett Jenkinson, Tanya L Schwab, Krutika Gaonkar, Margot A Cousin, Asha Nair, Shubham Basu, Pritha Chanana, Devin Oglesbee, Eric W Klee

    Published 2019-01-01
    Get full text
    Article
  2. 2
    Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy.

    Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy. by Eric D Wieben, Ross A Aleff, Shubham Basu, Vivekananda Sarangi, Brett Bowman, Ian J McLaughlin, John R Mills, Malinda L Butz, Edward W Highsmith, Cristiane M Ida, Jenny M Ekholm, Keith H Baratz, Michael P Fautsch

    Published 2019-01-01
    Get full text
    Article

Search Tools: