F. Erger
发表
M. Zaniew,
B. Hoppe,
M. Myślak,
2020,
Polish archives of internal medicine.
C. Becker,
P. Nürnberg,
J. Altmüller,
2020,
Genome Medicine.
M. Marlais,
M. Litwin,
L. Weber,
2020,
Scientific Reports.
A. Anarat,
S. Schmidt,
S. Testa,
2018,
The Journal of pediatrics.
Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up.
E. Salido,
B. Hoppe,
J. Groothoff,
2019,
Kidney international.
B. Schermer,
L. Weber,
H. Thiele,
2021,
Kidney international reports.
R. Heller,
P. Herkenrath,
B. Beck,
2017,
American journal of medical genetics. Part A.
B. McNicholas,
C. Becker,
P. Nürnberg,
2022
.
A. O’Donnell-Luria,
N. Chassaing,
C. Schaaf,
2021,
Journal of Medical Genetics.
William E. Byrd,
Gabor T. Marth,
David R. Murdock,
2020,
Genetics in Medicine.
M. Hallek,
P. Nürnberg,
J. Altmüller,
2021,
EMBO molecular medicine.
K. Zerres,
U. Gembruch,
N. O. Brüchle,
2017,
Archives of Gynecology and Obstetrics.
Tzung-Chien Hsieh,
P. Krawitz,
C. Gilissen,
2019,
American journal of human genetics.
J. Rosenfeld,
S. Ellard,
F. Alkuraya,
2019,
American journal of human genetics.
C. Schaaf,
C. Stumpel,
B. Horsthemke,
2020,
Orphanet Journal of Rare Diseases.
B. Hoppe,
J. Groothoff,
H. Peters-Sengers,
2019
.
K. Zerres,
L. Weber,
D. Mekahli,
2021,
Kidney international.
R. Müller,
E. Hahnen,
M. Liebau,
2022,
Kidney international reports.
B. McNicholas,
C. Becker,
P. Nürnberg,
2022,
The Journal of molecular diagnostics : JMD.
L. Weber,
B. Beck,
C. Taylan,
2020,
Frontiers in Pediatrics.
J. Schreml,
C. Netzer,
F. Erger,
2021,
Medizinische Genetik.
Markus M. Rinschen,
C. Becker,
J. Altmüller,
2023,
Genome Medicine.
C. Schaaf,
C. Netzer,
F. Erger,
2019,
Molecular and cellular probes.
R. Cummings,
L. Weber,
J. Altmüller,
2023,
Proceedings of the National Academy of Sciences of the United States of America.
R. Müller,
T. Benzing,
R. Gansevoort,
2023,
Clinical kidney journal.