Showing 1 - 4 results of 4 for search 'Stephanie Andres', query time: 0.03s Refine Results
  1. 1
    MAP2 – A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34

    MAP2 – A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34 by Dominik S. Westphal, Dominik S. Westphal, Stephanie Andres, Christine Makowski, Thomas Meitinger, Thomas Meitinger, Julia Hoefele

    Published 2018-03-01
    Get full text
    Article
  2. 2
    Genome wide noninvasive prenatal testing detects microduplication of the distal end of chromosome 15 in a fetus: a case report

    Genome wide noninvasive prenatal testing detects microduplication of the distal end of chromosome 15 in a fetus: a case report by Hana Sahinbegovic, Stephanie Andres, Sabine Langer-Freitag, Aspasia Divane, Fotini Ieremiadou, Senad Mehmedbasic, Aida Catic

    Published 2022-04-01
    Get full text
    Article
  3. 3
    Increased Radiation Sensitivity in Patients with Phelan-McDermid Syndrome

    Increased Radiation Sensitivity in Patients with Phelan-McDermid Syndrome by Sarah Jesse, Lukas Kuhlmann, Laura S. Hildebrand, Henriette Magelssen, Martina Schmaus, Beate Timmermann, Stephanie Andres, Rainer Fietkau, Luitpold V. Distel

    Published 2023-03-01
    Get full text
    Article
  4. 4
    Neurodegeneration or dysfunction in Phelan-McDermid syndrome? A multimodal approach with CSF and computational MRI

    Neurodegeneration or dysfunction in Phelan-McDermid syndrome? A multimodal approach with CSF and computational MRI by Sarah Jesse, Hans-Peter Müller, Hans-Jürgen Huppertz, Stephanie Andres, Albert C. Ludolph, Michael Schön, Tobias M. Boeckers, Jan Kassubek

    Published 2023-09-01
    Get full text
    Article

Search Tools: