Hasil Pencarian - Magdalena Danyel
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Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report oleh Magdalena Danyel, Eun Kyung Suk, Vera Raile, Jutta Gellermann, Alexej Knaus, Denise Horn
Diterbitkan 2019-01-01
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Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study oleh Alisa Maria Vittoria Reiter, Jean Tori Pantel, Magdalena Danyel, Denise Horn, Claus-Eric Ott, Martin Atta Mensah
Diterbitkan 2024-03-01
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Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy oleh Svea Horn, Svea Horn, Magdalena Danyel, Magdalena Danyel, Nina Erdmann, Nina Erdmann, Felix Boschann, Felix Boschann, Cecilia Gunnarsson, Cecilia Gunnarsson, Cecilia Gunnarsson, Saskia Biskup, Jerome Juengling, Cornelia Potratz, Cornelia Potratz, Christine Prager, Christine Prager, Angela M. Kaindl, Angela M. Kaindl, Angela M. Kaindl
Diterbitkan 2023-01-01
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4
Three-Dimensional Histological Characterization of the Placental Vasculature Using Light Sheet Microscopy oleh Lennart Freise, Rose Yinghan Behncke, Hanna Helene Allerkamp, Tim Henrik Sandermann, Ngoc Hai Chu, Eva Maria Funk, Lukas Jonathan Hondrich, Alina Riedel, Christian Witzel, Nils Rouven Hansmeier, Magdalena Danyel, Alexandra Gellhaus, Ralf Dechend, René Hägerling
Diterbitkan 2023-06-01
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