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
Gyftodimou, Yolanda
20
results:
Search for persons
X
Format
Online (20)
Mediatypes
Articles (Online) (14)
OpenAccess-fulltext (6)
Sorted by: Relevance
Sorted by: Year
?
1
CHD2 pathogenic nonsense variant in a three-generation fami..:
Angelopoulou, Eleni
;
Theodosiou, Athina
;
Papaevripidou, Ioannis
...
Heliyon. 9 (2023) 12 - p. e22987 , 2023
Link:
https://doi.org/10.1016/..
?
2
De novo 393kb microdeletion of 7p11.2 characterized by aCGH..:
Varvagiannis, Konstantinos
;
Papoulidis, Ioannis
;
Koromila, Theodora
...
Meta Gene. 2 (2014) - p. 274-282 , 2014
Link:
https://doi.org/10.1016/..
?
3
Loss-of-function HDAC8 mutations cause a phenotypic spectru..:
Kaiser, Frank J.
;
Ansari, Morad
;
Braunholz, Diana
...
Human Molecular Genetics. 23 (2014) 11 - p. 2888-2900 , 2014
Link:
https://doi.org/10.1093/..
?
4
Pure de novo partial trisomy 6p in a girl with craniosynost..:
Varvagiannis, Konstantinos
;
Stefanidou, Amalia
;
Gyftodimou, Yolanda
...
American Journal of Medical Genetics Part A. 161 (2013) 2 - p. 343-351 , 2013
Link:
https://doi.org/10.1002/..
?
5
Helical mutations in type I collagen that affect the proces..:
Malfait, Fransiska
;
Symoens, Sofie
;
Goemans, Nathalie
...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. 78 , 2013
Link:
https://doi.org/10.1186/..
?
6
A 725 kb deletion at 22q13.1 chromosomal region including S..:
Siomou, Elisavet
;
Manolakos, Emmanouil
;
Petersen, Michael
...
European Journal of Medical Genetics. 55 (2012) 11 - p. 641-645 , 2012
Link:
https://doi.org/10.1016/..
?
7
HDAC8 mutations in Cornelia de Lange syndrome affect the co..:
Deardorff, Matthew A.
;
Bando, Masashige
;
Nakato, Ryuichiro
...
Nature. 489 (2012) 7415 - p. 313-317 , 2012
Link:
https://doi.org/10.1038/..
?
8
Congenital hypothyroidism as the initial presentation that ..:
Dimitriadou, Meropi
;
Christoforidis, Athanasios
;
Sarri, Catherine
..
Gene. 494 (2012) 1 - p. 102-104 , 2012
Link:
https://doi.org/10.1016/..
?
9
Complex distal 10q rearrangement in a girl with mild intell..:
Sarri, Catherine
;
Douzgou, Sofia
;
Gyftodimou, Yolanda
...
American Journal of Medical Genetics Part A. 155 (2011) 11 - p. 2841-2854 , 2011
Link:
https://doi.org/10.1002/..
?
10
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJ..:
Kokotas, Haris
;
Grigoriadou, Maria
;
Yang, Li
...
International Journal of Pediatric Otorhinolaryngology. 75 (2011) 1 - p. 89-94 , 2011
Link:
https://doi.org/10.1016/..
?
11
Cohen syndrome resulting from a novel large intragenic COH1..:
Bugiani, Marianna
;
Gyftodimou, Yolanda
;
Tsimpouka, Paraskevi
...
American Journal of Medical Genetics Part A. 146A (2008) 17 - p. 2221-2226 , 2008
Link:
https://doi.org/10.1002/..
?
12
Wolf–Hirschhorn syndrome-associated chromosome changes are ..:
Zollino, Marcella
;
Lecce, Rosetta
;
Murdolo, Marina
...
Human Genetics. 123 (2008) 3 - p. 319-319 , 2008
Link:
https://doi.org/10.1007/..
?
13
Wolf–Hirschhorn syndrome-associated chromosome changes are ..:
Zollino, Marcella
;
Lecce, Rosetta
;
Murdolo, Marina
...
Human Genetics. 122 (2007) 5 - p. 423-430 , 2007
Link:
https://doi.org/10.1007/..
?
14
Prenatal diagnosis of glycogen storage disease type IV:
Akman, H. Orhan
;
Karadimas, Charalampos
;
Gyftodimou, Yolanda
...
Prenatal Diagnosis. 26 (2006) 10 - p. 951-955 , 2006
Link:
https://doi.org/10.1002/..
?
15
Loss-of-function HDAC8 mutations cause a phenotypic spectru..:
Kaiser, Frank J
;
Ansari, Morad
;
Braunholz, Diana
...
boreal:164111. , 2014
Link:
http://hdl.handle.net/20..
1-15