Bilaketaren emaitzak - Gallant, Emily

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  1. 1
    Homozygosity for the V37I GJB2 Mutation in Fifteen Probands with Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in Asian Populations

    Homozygosity for the V37I GJB2 Mutation in Fifteen Probands with Mild to Moderate Sensorineural Hearing Impairment: Further Confirmation of Pathogenicity and Haplotype Analysis in... nork Gallant, Emily, Francey, Lauren, Tsai, Ellen A., Berman, Micah, Zhao, Yaru, Fetting, Heather, Kaur, Maninder, Deardorff, Matthew A., Wilkens, Alisha, Clark, Dinah, Hakonarson, Hakon, Rehm, Heidi, Krantz, Ian D.

    Argitaratua 2013
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  2. 2
    Semaphorin 3d signaling defects are associated with anomalous pulmonary venous connections

    Semaphorin 3d signaling defects are associated with anomalous pulmonary venous connections nork Degenhardt, Karl, Singh, Manvendra K, Aghajanian, Haig, Massera, Daniele, Wang, Qiaohong, Li, Jun, Li, Li, Choi, Connie, Yzaguirre, Amanda D, Francey, Lauren J, Gallant, Emily, Krantz, Ian D, Gruber, Peter J, Epstein, Jonathan A

    Argitaratua 2013
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  3. 3
    PECONPI: A Novel Software for Uncovering Pathogenic Copy Number Variations in Non-Syndromic Sensorineural Hearing Loss and Other Genetically Heterogeneous Disorders

    PECONPI: A Novel Software for Uncovering Pathogenic Copy Number Variations in Non-Syndromic Sensorineural Hearing Loss and Other Genetically Heterogeneous Disorders nork Tsai, Ellen A, Berman, Micah A, Conlin, Laura K, Rehm, Heidi L, Francey, Lauren J, Deardorff, Matthew A, Holst, Jenelle, Kaur, Maninder, Gallant, Emily, Clark, Dinah M, Glessner, Joseph T, Jensen, Shane T, Grant, Struan FA, Gruber, Peter J, Hakonarson, Hakon, Spinner, Nancy B, Krantz, Ian D

    Argitaratua 2013
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