T. Eisenberger
发表
U. Zimmermann,
M. Knipper,
H. Bolz,
2017,
Clinical genetics.
T. Eisenberger,
C. Bergmann,
C. Decker,
2015,
PloS one.
A. Baiker,
H. Lipps,
T. Eisenberger,
2004,
Proceedings of the National Academy of Sciences of the United States of America.
R. Lovell-Badge,
A. Cooney,
D. Riethmacher,
2009,
Cell.
J. Al-Aama,
B. Lorenz,
T. Neuhann,
2013,
PloS one.
T. Eisenberger,
C. Bergmann,
H. Bolz,
2014,
British Journal of Ophthalmology.
A. Baiker,
H. Lipps,
T. Eisenberger,
2005,
Human gene therapy.
Colin A. Johnson,
H. Bolz,
B. Schermer,
2013,
Human molecular genetics.
T. Eisenberger,
Ulrich Elling,
Katrin Anlag,
2006,
Proceedings of the National Academy of Sciences.
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
M. Boerries,
I. Wilson,
T. Eisenberger,
2022,
American journal of human genetics.
H. Bolz,
C. Neuhaus,
T. Eisenberger,
2017,
Genetics in Medicine.
S. Lenzner,
P. Charbel Issa,
C. Neuhaus,
2018,
PloS one.
B. Lorenz,
H. Stöhr,
P. Charbel Issa,
2017,
Molecular genetics & genomic medicine.
K. Steel,
M. Ptok,
U. Zimmermann,
2015,
Orphanet Journal of Rare Diseases.
C. Neuhaus,
T. Eisenberger,
C. Bergmann,
2014,
Human mutation.
M. Hurles,
P. Scambler,
T. Neuhann,
2013,
Human mutation.
S. Lenzner,
P. Charbel Issa,
C. Neuhaus,
2018,
Scientific Reports.
R. Roepman,
N. Sebire,
M. Ueffing,
2013,
Nature Genetics.
Carsten Bergmann,
Martin Pohl,
T. Eisenberger,
2014,
Pediatric Nephrology.
Carsten Bergmann,
Peter Nürnberg,
Ahmad Mansour,
2012,
Orphanet Journal of Rare Diseases.
Yang Wang,
Monte Westerfield,
Carsten Bergmann,
2014,
Human mutation.
U. Wolfrum,
H. Bolz,
K. Nagel-Wolfrum,
2015,
British Journal of Ophthalmology.
H. Bolz,
F. Alkuraya,
T. Eisenberger,
2013,
British Journal of Ophthalmology.
Sophie,
R. Roepman,
N. Sebire,
2013
.