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Xiaowu Gai

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  1. "2012"
Formats
  1. Journal Article (3)
Years
  1. 2012 (3)
Journals
  1. Bipolar disorders (1)
  2. Discovery medicine (1)
  3. Nature genetics (1)
Publishers
  1. Wiley Periodicals, Inc (1)

Results (3)

  • Re-sequencing of ankyrin 3 exon 48 and case-control association analysis of rare variants in bipolar disorder type I
    Journal Article

    Doyle, G. A.; Lai, A. T.; Chou, A. D.; Wang, M. J.; Gai, X.; Rappaport, E. F.; Berrettini, W. H.
    Bipolar disorders (2012)

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  • Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome
    Journal Article

    Falk, M. J.; Pierce, E. A.; Consugar, M.; Xie, M. H.; Guadalupe, M.; Hardy, O.; Rappaport, E. F.; Wallace, D. C.; LeProust, E.; Gai, X.
    Discovery medicine (2012)

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  • NMNAT1 mutations cause Leber congenital amaurosis
    Journal Article

    Falk, M. J.; Zhang, Q.; Nakamaru-Ogiso, E.; Kannabiran, C.; Fonseca-Kelly, Z.; Chakarova, C.; Audo, I.; Mackay, D. S.; Zeitz, C.; Borman, A. D.; more...
    Nature genetics (2012)

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