Hasil Pencarian - Gertrud Strobl‐Wildemann

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    Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome

    Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome oleh Dennis Witt, Ulrike Faust, Gertrud Strobl‐Wildemann, Marc Sturm, Rebecca Buchert, Theresia Zuleger, Jakob Admard, Nicolas Casadei, Stephan Ossowski, Tobias B. Haack, Olaf Rieß, Christopher Schroeder

    Diterbitkan 2023-06-01
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