Search Results - Witt, Mariah A.

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  1. 1
    Ending a diagnostic odyssey: Moving from exome to genome to identify cockayne syndrome

    Ending a diagnostic odyssey: Moving from exome to genome to identify cockayne syndrome by Friedman, Jennifer, Bird, Lynne M., Haas, Richard, Robbins, Shira L., Nahas, Shareef A., Dimmock, David P., Yousefzadeh, Matthew J., Witt, Mariah A., Niedernhofer, Laura J., Chowdhury, Shimul

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  2. 2
    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A

    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A by García-Carmona, Juan Antonio, Yousefzadeh, Matthew J., Alarcón-Soldevilla, Fernando, Fages-Caravaca, Eva, Kieu, Tra L., Witt, Mariah A., López-Ávila, Ángel, Niedernhofer, Laura J., Pérez-Vicente, José Antonio

    Published in Frontiers in genetics
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    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A

    Case Report: Identification of a Heterozygous XPA c.553C>T Mutation Causing Neurological Impairment in a Case of Xeroderma Pigmentosum Complementation Group A by García-Carmona, Juan Antonio, Yousefzadeh, Matthew J, Alarcón-Soldevilla, Fernando, Fages-Caravaca, Eva, Kieu, Tra L, Witt, Mariah A, López-Ávila, Ángel, Niedernhofer, Laura J, Pérez-Vicente, José Antonio

    Published in Frontiers in genetics
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    The Impact of Resident Geographic Rounding on Rapid Responses

    The Impact of Resident Geographic Rounding on Rapid Responses by Williams, Alexander, DeMott, Chad, Whicker, Shari, Rudd, Mariah, Lockhart, Ellen Rachel, Isanaka, Pavan, Witt, Christa

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