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
Zeybek, Selcan
10
results:
Search for persons
X
Format
Online (10)
Mediatypes
Articles (Online) (2)
OpenAccess-fulltext (8)
Languages
english (9)
Sorted by: Relevance
Sorted by: Year
?
1
Severe microcephaly and rapid deterioration due to cortical..:
Olmez, Akgun
;
Zeybek, Selcan
Annals of Indian Academy of Neurology. 25 (2022) 4 - p. 735 , 2022
Link:
https://doi.org/10.4103/..
?
2
A Novel Homozygous GALK1 Variant Combined With Cataract and..:
Ozler, Oguz
;
Egeli, Bugra Han
;
Zeybek, Selcan
..
Clinical Pediatrics. 62 (2022) 6 - p. 537-540 , 2022
Link:
https://doi.org/10.1177/..
?
3
Further delineation of ACPHD syndrome and a novel mutation ..:
Öztürk, Menekşe
;
Zeybek, Selcan
;
Farre, G
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
4
A Novel Nonsense Mutation In The EYA1 Gene Found In A Patie..:
Albuz, Burcu
;
Zeybek, Selcan
;
Anlas, Özlem
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
5
The co-existence of Nablus Mask-Like Facial Syndrome and Kl..:
Anlaş, Özlem
;
Sarikepe, B
;
Zeybek, Selcan
...
EUROPEAN JOURNAL OF HUMAN GENETICS. , 2019
Link:
https://hdl.handle.net/1..
?
6
Co-existence of Goldenhar and Klinefelter Syndromes in a Pa..:
Zeybek, Selcan
;
Sarıkepe, Bilge
;
Bağcı, Gülseren
..
Erciyes Medical Journal. , 2018
Link:
https://hdl.handle.net/1..
?
7
Familial mutation in caffey disease with reduced penetrance..:
Özdemir, Özmert Muhammet Ali
;
Tancer-Elçi, Hazal
;
Polat, Aziz
...
Turkish Journal of Pediatrics. , 2017
Link:
https://hdl.handle.net/1..
?
8
Familial mutation in Caffey disease with reduced penetrance..:
Ayaz, Akif
;
Özdemir, Özmert M. A
;
Tancer-Elçi, Hazal
...
Turkish Journal of Pediatrics. , 2016
Link:
https://hdl.handle.net/1..
?
9
Tekrarlayan gebelik kaybı olan vakalarda pentraxin 3 ekspre..:
Zeybek, Selcan
Tez. , 2015
Link:
https://hdl.handle.net/1..
?
10
Severe microcephaly and rapid deterioration due to cortical..:
Akgun Olmez
;
Selcan Zeybek
http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=4;spage=735;epage=738;aulast=Olmez. , 2022
Link:
https://doi.org/10.4103/..
1-10