Cordula Knopp

Publication Activity (10 Years)

Years Active: 2021-2021
Publications (10 Years): 1

Top Topics

Intellectual Disability

Magnetic Resonance Imaging

Duchenne Muscular Dystrophy

Top Venues

European journal of human genetics : EJHG

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

Publications

Natja Haag, Ene Choo Tan, Matthias Begemann, Lars Buschmann, Florian Kraft, Petra Holschbach, Angeline H M Lai, Maggie Brett, Ganeshwaran H Mochida, Stephanie DiTroia, Lynn Pais, Jennifer E Neil, Muna Al-Saffar, Laila Bastaki, Christopher A Walsh, Ingo Kurth, Cordula Knopp
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European journal of human genetics : EJHG 29 (11) (2021)