Hasil Pencarian - Shelby Geilmann

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  1. 1
    P172: Novel biallelic variants in the CSMD1 gene in a child with cerebellar ataxia and developmental regression: A case report

    P172: Novel biallelic variants in the CSMD1 gene in a child with cerebellar ataxia and developmental regression: A case report oleh Shelby Geilmann, Brian Shayota

    Diterbitkan 2023-01-01
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  2. 2
    A novel RAD51 variant resulting in Fanconi anemia identified in an infant with multiple congenital anomalies

    A novel RAD51 variant resulting in Fanconi anemia identified in an infant with multiple congenital anomalies oleh Shelby Geilmann, Rachel Solstad, Rachel Palmquist, Josue Flores Daboub, Lorenzo D. Botto, Peter H. Grubb, Josh L. Bonkowsky, Nicola Longo, Sabrina Malone Jenkins

    Diterbitkan 2023-01-01
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