Arama Sonuçları - Branch, Justin

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  1. 1
    Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy

    Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy Yazar: Porto, Fernanda B. O., Jones, Evan M., Branch, Justin, Soens, Zachry T., Maia, Igor Mendes, Sena, Isadora F. G., Sampaio, Shirley A. M., Simões, Renata T., Chen, Rui

    Baskı/Yayın Bilgisi 2017
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  2. 2
    A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome

    A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome Yazar: Chaimowitz, Natalia S., Branch, Justin, Reyes, Anaid, Vargas-Hernández, Alexander, Orange, Jordan S., Forbes, Lisa R., Ehlayel, Mohammed, Purayil, Saleema C., Al-Nesf, Maryam Ali, Vogel, Tiphanie P.

    Baskı/Yayın Bilgisi 2019
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  3. 3
    Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants amongst exon-captured variants of uncertain significance

    Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants amongst exon-captured variants of uncertain significa... Yazar: Soens, Zachry T., Branch, Justin, Wu, Shijing, Yuan, Zhisheng, Li, Yumei, Li, Hui, Wang, Keqing, Xu, Mingchu, Rajan, Lavan, Motta, Fabiana L., Simões, Renata T., Lopez-Solache, Irma, Ajlan, Radwan, Birch, David G., Zhao, Peiquan, Porto, Fernanda B., Sallum, Juliana, Koenekoop, Robert K., Sui, Ruifang, Chen, Rui

    Baskı/Yayın Bilgisi 2017
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