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Sarah Verheyen

Showing results (1-10 of 17) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Christine Fauth, Sarah Verheyen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 6, 2024
Sarah Verheyen, Ellen Heitzer, Jochen Geigl
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|December 4, 2019
The Fetal Posterior Fossa on Prenatal Ultrasound Imaging: Normal Longitudinal Development and Posterior Fossa AnomaliesBarbara Pertl, Sophie Eder, Christina Stern, et al.
Neurology. Genetics|August 18, 2020
Childhood-onset epileptic encephalopathy due to <i>FGF12</i> exon 1-4 tandem duplicationSarah Verheyen, Michael R Speicher, Barbara Ramler, et al.
Patient Education and Counseling|May 3, 2016
Medication adherence among pregnant women with hypothyroidism-missed opportunities to improve reproductive health? A cross-sectional, web-based studyHerbert Juch, Angela Lupattelli, Eivind Ystrom, et al.
Research in Developmental Disabilities|March 3, 2019
Early motor and pre-linguistic verbal development in Prader-Willi syndrome - A case reportJasmin Pansy, Cornelia Barones, Berndt Urlesberger, et al.
European Journal of Medical Genetics|November 15, 2022
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delayMelissa Rieger, Sébastien Moutton, Sarah Verheyen, et al.
Genes|October 23, 2021
Myocardial Deformation Analysis in <i>MYBPC3</i> and <i>MYH7</i> Related Sarcomeric Hypertrophic Cardiomyopathy-The Graz Hypertrophic Cardiomyopathy RegistryViktoria Höller, Heidelis Seebacher, David Zach, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Sarah Verheyen, Barbara Pertl, Sophie Bierbaumer, et al.
Journal of Medical Genetics|August 11, 2021
Biallelic truncating variants in <i>ATP9A</i> cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thriveGuido Vogt, Sarah Verheyen, Sarina Schwartzmann, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Christine Fauth, Sarah Verheyen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 6, 2024
Sarah Verheyen, Ellen Heitzer, Jochen Geigl
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|December 4, 2019
The Fetal Posterior Fossa on Prenatal Ultrasound Imaging: Normal Longitudinal Development and Posterior Fossa AnomaliesBarbara Pertl, Sophie Eder, Christina Stern, et al.
Neurology. Genetics|August 18, 2020
Childhood-onset epileptic encephalopathy due to <i>FGF12</i> exon 1-4 tandem duplicationSarah Verheyen, Michael R Speicher, Barbara Ramler, et al.
Patient Education and Counseling|May 3, 2016
Medication adherence among pregnant women with hypothyroidism-missed opportunities to improve reproductive health? A cross-sectional, web-based studyHerbert Juch, Angela Lupattelli, Eivind Ystrom, et al.
Research in Developmental Disabilities|March 3, 2019
Early motor and pre-linguistic verbal development in Prader-Willi syndrome - A case reportJasmin Pansy, Cornelia Barones, Berndt Urlesberger, et al.
European Journal of Medical Genetics|November 15, 2022
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delayMelissa Rieger, Sébastien Moutton, Sarah Verheyen, et al.
Genes|October 23, 2021
Myocardial Deformation Analysis in <i>MYBPC3</i> and <i>MYH7</i> Related Sarcomeric Hypertrophic Cardiomyopathy-The Graz Hypertrophic Cardiomyopathy RegistryViktoria Höller, Heidelis Seebacher, David Zach, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Sarah Verheyen, Barbara Pertl, Sophie Bierbaumer, et al.
Journal of Medical Genetics|August 11, 2021
Biallelic truncating variants in <i>ATP9A</i> cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thriveGuido Vogt, Sarah Verheyen, Sarina Schwartzmann, et al.
Pageof 2