Jan Hendrik Niemann

Publication Activity (10 Years)

Years Active: 2020-2020
Publications (10 Years): 1

Top Topics

Patient Reported

Autism Spectrum Disorder

Ejection Fraction

Top Venues

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Jan Hendrik Niemann, Chen Du, Susanne Morlot, Gunnar Schmidt, Bernd Auber, Beate Kaune, Gudrun Göhring, Tim Ripperger, Brigitte Schlegelberger, Winfried Hofmann, Thomas Smol, Emilie Ait-Yahya, Anna Raimbault, Anne Lambilliotte, Florence Petit, Doris Steinemann
De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia. Clinical genetics 98 (4) (2020)