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
Kurtas, Nehir Edibe
18
results:
Search for persons
X
Format
Online (18)
Mediatypes
Articles (Online) (9)
Bookchapter (Online) (2)
OpenAccess-fulltext (7)
Sorted by: Relevance
Sorted by: Year
?
1
22q11.2 deletion syndrome: Future directions:
, In:
The Chromosome 22q11.2 Deletion Syndrome
,
Vermeesch, Joris Robert
;
Kurtas, Nehir Edibe
- p. 406-418 , 2022
Link:
https://doi.org/10.1016/..
?
2
Integration of Hi-C with short and long-read genome sequenc..:
Schöpflin, Robert
;
Melo, Uirá Souto
;
Moeinzadeh, Hossein
...
Nature Communications. 13 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
3
Contributors:
, In:
The Chromosome 22q11.2 Deletion Syndrome
,
Bassett, Anne S.
;
Van Batavia, Jason P.
;
Boot, Erik
... - p. xv-xvii , 2022
Link:
https://doi.org/10.1016/..
?
4
Chiari 1 malformation and exome sequencing in 51 trios: the..:
Provenzano, Aldesia
;
La Barbera, Andrea
;
Scagnet, Mirko
...
Human Genetics. 140 (2020) 4 - p. 625-647 , 2020
Link:
https://doi.org/10.1007/..
?
5
Small supernumerary marker chromosomes: A legacy of trisomy..:
Kurtas, Nehir Edibe
;
Xumerle, Luciano
;
Leonardelli, Lorena
...
Human Mutation. 40 (2018) 2 - p. 193-200 , 2018
Link:
https://doi.org/10.1002/..
?
6
De novo unbalanced translocations have a complex history/ae..:
Bonaglia, Maria Clara
;
Kurtas, Nehir Edibe
;
Errichiello, Edoardo
...
Human Genetics. 137 (2018) 10 - p. 817-829 , 2018
Link:
https://doi.org/10.1007/..
?
7
SOX2: Not always eye malformations. Severe genital but no m..:
Errichiello, Edoardo
;
Gorgone, Cristina
;
Giuliano, Loretta
...
European Journal of Medical Genetics. 61 (2018) 6 - p. 335-340 , 2018
Link:
https://doi.org/10.1016/..
?
8
Insertional translocation involving an additional nonchromo..:
Kurtas, Nehir Edibe
;
Xumerle, Luciano
;
Giussani, Ursula
...
Molecular Genetics & Genomic Medicine. 7 (2018) 2 - p. , 2018
Link:
https://doi.org/10.1002/..
?
9
Integration of Hi-C with short and long-read genome sequenc..:
Schöpflin, Robert
;
Melo, Uirá Souto
;
Moeinzadeh, Hossein
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617858/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
10
Integration of Hi-C with short and long-read genome sequenc..:
Schöpflin, Robert
;
Melo, Uirá Souto
;
Moeinzadeh, Hossein
...
https://pure.au.dk/portal/da/publications/integration-of-hic-with-short-and-longread-genome-sequencing-reveals-the-structure-of-germline-rearranged-genomes(2bf0568a-6234-433b-a725-b64e0a62318e).html. , 2022
Link:
https://pure.au.dk/porta..
?
11
Chiari 1 malformation and exome sequencing in 51 trios: the..:
Provenzano, Aldesia
;
La Barbera, Andrea
;
Scagnet, Mirko
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981314/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
12
Small supernumerary marker chromosomes: A legacy of trisomy..:
Kurtas, Nehir Edibe
;
Xumerle, Luciano
;
Leonardelli, Lorena
...
info:eu-repo/semantics/altIdentifier/pmid/30412329. , 2019
Link:
http://hdl.handle.net/23..
?
13
SOX2: Not always eye malformations. Severe genital but no m..:
Errichiello, Edoardo
;
Gorgone, Cristina
;
Giuliano, Loretta
...
info:eu-repo/semantics/altIdentifier/pmid/29371155. , 2018
Link:
http://hdl.handle.net/11..
?
14
Small supernumerary marker chromosomes: a legacy of trisomy..:
KURTAS, EDIBE NEHIR
http://hdl.handle.net/11571/1231926. , 2019
Link:
http://hdl.handle.net/11..
?
15
Integration of Hi-C with short and long-read genome sequenc..:
Robert Schöpflin
;
Uirá Souto Melo
;
Hossein Moeinzadeh
...
https://doi.org/10.1038/s41467-022-34053-7. , 2022
Link:
https://doi.org/10.1038/..
1-15
