I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Ityel, Hadas
11
results:
OpenAccess-fulltext X
Search for persons
X
Sorted by: Relevance
Sorted by: Year
?
1
Mutations of the Transcriptional Corepressor ZMYM2 Cause Sy..:
Connaughton, Dervla M
;
Dai, Rufeng
;
Owen, Danielle J
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536580/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
2
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Rec..:
Mann, Nina
;
Kause, Franziska
;
Henze, Erik K
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904809/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
3
Monogenic causes of chronic kidney disease in adults:
Connaughton, Dervla M
;
Kennedy, Claire
;
Shril, Shirlee
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431580/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
4
Whole-Exome Sequencing Identifies Causative Mutations in Fa..:
van der Ven, Amelie T
;
Connaughton, Dervla M
;
Ityel, Hadas
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115658/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
5
Whole Exome Sequencing of Patients with Steroid-Resistant N..:
Ferguson, Michael A
;
Ozaltin, FATİH
;
Hildebrandt, Friedhelm
...
3d47d3cc-714a-40ec-94b2-2a70e3fe0288. , 2018
Link:
https://doi.org/10.2215/..
?
6
Whole Exome Sequencing of Patients with Steroid-Resistant N..:
Warejko, Jillian K
;
Tan, Weizhen
;
Daga, Ankana
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753307/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
7
Exome sequencing in Jewish and Arabic patients with rhabdom..:
Vivante, Asaf
;
Ityel, Hadas
;
Pode-Shakked, Ben
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903869/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
8
Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinical..:
van der Ven, Amelie T
;
Shril, Shirlee
;
Ityel, Hadas
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582506/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
9
A Dominant Mutation in Nuclear Receptor Interacting Protein..:
Vivante, Asaf
;
Mann, Nina
;
Yonath, Hagith
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533226/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
10
A Dominant Negative Heterozygous G87R Mutation in the Zinc ..:
Lasry, Inbal
;
Seo, Young Ah
;
Ityel, Hadas
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436150. , 2012
Link:
http://www.ncbi.nlm.nih...
?
11
A homozygous missense variant in VWA2, encoding an interact..:
Amelie T van der Ven
;
Birgit Kobbe
;
Stefan Kohl
...
http://europepmc.org/articles/PMC5774751?pdf=render. , 2018
Link:
https://doi.org/10.1371/..
1-11