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Neuropediatrics
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October 21, 2020
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters
Eva-Katharina Willimsky, Anna Munzig, Karin Mayer, et al.
Human Molecular Genetics
|
May 21, 2019
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Marialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, et al.
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Search research articles
Search
Showing results (1-10 of 2) with videos related to
Sort By:
Page
of 1
Neuropediatrics
|
October 21, 2020
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters
Eva-Katharina Willimsky, Anna Munzig, Karin Mayer, et al.
Human Molecular Genetics
|
May 21, 2019
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Marialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, et al.
Page
of 1