Stefanie Beck-Woedl
发表
H. Mefford,
Y. Marie,
S. Sisodiya,
2016,
Journal of Medical Genetics.
T. Bast,
C. Schaaf,
T. Haack,
2021,
Human mutation.
E. Ringelstein,
T. Strom,
H. Lerche,
2019,
Annals of clinical and translational neurology.
A. Pagnamenta,
M. Nieto,
Z. Tümer,
2023,
European Journal of Human Genetics.
Niklas Luetzen,
T. Haack,
A. Tzschach,
2023,
American journal of medical genetics. Part A.
T. Haack,
G. Stoltenburg‐Didinger,
S. Zierz,
2022,
Journal of neuromuscular diseases.
K. Kagan,
M. Hoopmann,
M. Sturm,
2022,
Prenatal diagnosis.
S. Groeschel,
V. Gieselmann,
G. Bruchelt,
2022,
JIMD reports.
S. Mane,
T. Nägele,
T. Meitinger,
2020,
American journal of human genetics.
D. Horn,
S. Mundlos,
B. Tüysüz,
2019,
Journal of Human Genetics.
H. Mefford,
Y. Marie,
S. Sisodiya,
2016,
Journal of Medical Genetics.
P. Bauer,
C. Evers,
C. Schroeder,
2015,
European Journal of Human Genetics.
R. Krüger,
A. Dufke,
O. Riess,
2013,
Clinical genetics.
V. Calbi,
A. Zerem,
Hanka Dekker,
2024,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
S. Groeschel,
K. Harzer,
I. Kraegeloh-Mann,
2019,
Neuropediatrics.