E-LIB Suche - Ergebnisse für: Stong, N.

1

P867: TUMOR PROFILING OF IDECABTAGENE VICLEUCEL (IDE-CEL; B..:

Martin, N. ; Xu, A. ; Stong, N....
HemaSphere. 6 (2022) - p. 760-761 , 2022

Link: https://doi.org/10.1097/..

2

P867: TUMOR PROFILING OF IDECABTAGENE VICLEUCEL (IDE-CEL; B..:

Martin, N ; Xu, A ; Stong, N...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429269/. , 2022

Link: http://www.ncbi.nlm.nih...

3

De novo variants in SNAP25 cause an early-onset development..:

Klöckner, C ; Sticht, H ; Zacher, P...
https://discovery.ucl.ac.uk/id/eprint/10117525/3/McTague_Manuscript_SNAP25_v16%20accepted%20version.pdf. , 2021

Link: https://discovery.ucl.ac..

4

Missense variants in the histone acetyltransferase complex ..:

Cogné, B ; Ehresmann, S ; Beauregard-Lacroix, E...
doi:10.1016/j.ajhg.2019.01.010. , 2021

Link: https://doi.org/10.1016/..

5

Coding and noncoding variants in EBF3 are involved in HADDS..:

Padhi, EM ; Hayeck, TJ ; Cheng, Z...
https://discovery.ucl.ac.uk/id/eprint/10132287/1/s40246-021-00342-3.pdf. , 2021

Link: https://discovery.ucl.ac..

6

Coding and noncoding variants in EBF3 are involved in HADDS..:

Padhi, EM ; Hayeck, TJ ; Cheng, Z...
https://openaccess.sgul.ac.uk/id/eprint/113548/1/s40246-021-00342-3.pdf. , 2021

Link: https://openaccess.sgul...

7

SSBP1 mutations cause mtDNA depletion underlying a complex ..:

Del Dotto, V ; Ullah, F ; Di Meo, I...
info:eu-repo/semantics/altIdentifier/doi/10.1172/JCI128514. , 2020

Link: https://push-zb.helmholt..

8

De novo variants in SNAP25 cause an early-onset development..:

Klöckner, C ; Sticht, H ; Zacher, P...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-01020-w. , 2020

Link: https://push-zb.helmholt..

9

Heterozygous loss-of-function variants of MEIS2 cause a tri..:

Verheije, R ; Kupchik, G.S ; Isidor, B...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41431-018-0281-5. , 2019

Link: https://push-zb.helmholt..

10

Autism and developmental disability caused by KCNQ3 gain-of..:

Sands T. T ; Miceli F ; Lesca G...
info:eu-repo/semantics/altIdentifier/wos/WOS:000475670500004. , 2019

Link: http://hdl.handle.net/11..

11

The Epilepsy Genetics Initiative: Systematic reanalysis of ..:

Berkovic, SF ; Goldstein, DB ; Heinzen, EL...
issn:0013-9580. , 2019

Link: http://hdl.handle.net/11..

12

Loss of tubulin deglutamylase CCP1 causes infantile-onset n..:

Shashi, V ; Magiera, M.M ; Klein, D...
info:eu-repo/semantics/altIdentifier/doi/10.15252/embj.2018100540. , 2018

Link: https://push-zb.helmholt..

13

De Novo Truncating Variants in ASXL2 Are Associated with a ..:

Shashi, V ; Pena, LD ; Kim, K...
American Journal of Human Genetics. , 2016

Link: http://hdl.handle.net/10..

14

P867: TUMOR PROFILING OF IDECABTAGENE VICLEUCEL (IDE-CEL; B..:

N. Martin ; A. Xu ; N. Stong...
http://journals.lww.com/10.1097/01.HS9.0000846348.62497.10. , 2022

Link: https://doi.org/10.1097/..

15

Ancestry adjustment improves genome-wide estimates of regio..:

Hayeck, Tristan J ; Stong, Nicholas ; Baugh, Evan...
Genetics. , 2022

Link: https://doi.org/10.1093/..