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Endele, S
28
results:
Search for persons
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Online (28)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (19)
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english (24)
german (3)
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?
1
Kirschner-Draht-Osteosynthese von Frakturen des Condylus ra..:
Fernandez, F.F.
;
Eberhardt, O.
;
von Kalle, T.
..
Obere Extremität. 4 (2009) 1 - p. 26-32 , 2009
Link:
https://doi.org/10.1007/..
?
2
LETM1, deleted in Wolf Hirschhorn syndrome is required for ..:
Dimmer, K. S.
;
Navoni, F.
;
Casarin, A.
...
Human Molecular Genetics. 17 (2007) 2 - p. 201-214 , 2007
Link:
https://doi.org/10.1093/..
?
3
The recurrent missense mutation p.(Arg367Trp) in YARS1 caus..:
Averdunk, L
;
Sticht, H
;
Surowy, H
...
https://discovery.ucl.ac.uk/id/eprint/10136448/1/Averdunk2021_Article_TheRecurrentMissenseMutationPA.pdf. , 2021
Link:
https://discovery.ucl.ac..
?
4
Mutations in the BAF-complex subunit DPF2 are associated wi..:
Vasileiou, G
;
Vergarajauregui, S
;
Endele, S
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2018.01.014. , 2018
Link:
https://push-zb.helmholt..
?
5
Mutations in the BAF-complex subunit DPF2 associated with C..:
Vasileiou, G
;
Vergarajauregui, S
;
Endele, S
...
doi:10.1016/j.ajhg.2018.01.014. , 2018
Link:
https://doi.org/10.1016/..
?
6
Loss-of-function variants in HIVEP2 are a cause of intellec..:
Srivastava, S
;
Engels, H
;
Schanze, I
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/ejhg.2015.151. , 2016
Link:
https://push-zb.helmholt..
?
7
In-Frame Deletion and Missense Mutations of the C-Terminal ..:
Wolff, D
;
Endele, S
;
Azzarello-Burri, S
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362220. , 2012
Link:
http://www.ncbi.nlm.nih...
?
8
Langzeitergebnisse nach intramedullärer Stabilisation von d..:
Fernandez, F
;
Endele, S
;
Eberhardt, O
.
http://dx.doi.org/10.3205/09dkou241. , 2009
Link:
https://doi.org/10.3205/..
?
9
Partial deletion of 4p and 4q in a fetus with ring chromoso..:
Kocks, A
;
Endele, S
;
Heller, R
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735105. , 2002
Link:
http://www.ncbi.nlm.nih...
?
10
The recurrent missense mutation p.(Arg367Trp) in YARS1 caus..:
Averdunk, Luisa
;
Sticht, Heinrich
;
Surowy, Harald
...
Journal of Molecular Medicine. 99 (2021) 12 - p. 1755-1768 , 2021
Link:
https://doi.org/10.1007/..
?
11
Correction to: The recurrent missense mutation p.(Arg367Trp..:
Averdunk, Luisa
;
Sticht, Heinrich
;
Surowy, Harald
...
Journal of Molecular Medicine. 99 (2021) 12 - p. 1769-1770 , 2021
Link:
https://doi.org/10.1007/..
?
12
Publisher Correction: Asymmetric lysosome inheritance predi..:
Loeffler, Dirk
;
Wehling, Arne
;
Schneiter, Florin
...
Nature. 573 (2019) 7775 - p. E5-E5 , 2019
Link:
https://doi.org/10.1038/..
?
13
Asymmetric lysosome inheritance predicts activation of haem..:
Loeffler, Dirk
;
Wehling, Arne
;
Schneiter, Florin
...
Nature. 573 (2019) 7774 - p. 426-429 , 2019
Link:
https://doi.org/10.1038/..
?
14
Early myeloid lineage choice is not initiated by random PU...:
Hoppe, Philipp S.
;
Schwarzfischer, Michael
;
Loeffler, Dirk
...
Nature. 535 (2016) 7611 - p. 299-302 , 2016
Link:
https://doi.org/10.1038/..
?
15
Software tools for single-cell tracking and quantification ..:
Hilsenbeck, Oliver
;
Schwarzfischer, Michael
;
Skylaki, Stavroula
...
Nature Biotechnology. 34 (2016) 7 - p. 703-706 , 2016
Link:
https://doi.org/10.1038/..
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