Hasil Pencarian - Keith Wetherby

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  1. 1
    Retrospective analysis in oculocutaneous albinism patients for the 2.7 kb deletion in the OCA2 gene revealed a co-segregation of the controversial variant, p.R305W

    Retrospective analysis in oculocutaneous albinism patients for the 2.7 kb deletion in the OCA2 gene revealed a co-segregation of the controversial variant, p.R305W oleh Jackson Gao, Leera D’Souza, Keith Wetherby, Christian Antolik, Melissa Reeves, David R. Adams, Santa Tumminia, Xinjing Wang

    Diterbitkan 2017-04-01
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  2. 2
    Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophies

    Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophies oleh Xinjing Wang, Wadih M. Zein, Leera D’Souza, Chimere Roberson, Keith Wetherby, Hong He, Angela Villarta, Amy Turriff, Kory R. Johnson, Yang C. Fann

    Diterbitkan 2017-08-01
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