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Single Center Experience with Diagnostic Whole Genome Sequencing in 70 Patients with Rare Diseases

Doreen William, Zarah Kowalzyk,Karl Hackmann, Marion Bermudez, Oliver Kutz, Samira Zarvandi,Jan Fischer, Arne Jahn, Marcus Franke, Maria Constanza Roa Bravo, Lydia Rossow, Ann-Selin Onuk, Sylvia Huetter,Joseph Porrmann,Jens Schallner,Tanita Kretschmer, Catharina Schuetz, Min Ae Lee-Kirsch,Reinhard Berner,Evelin Schroeck, Nataliya Di Donato

EUROPEAN JOURNAL OF HUMAN GENETICS(2024)

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