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
Chijiwa, Chieko
21
results:
english X
Search for persons
X
Format
Online (21)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (12)
Sorted by: Relevance
Sorted by: Year
?
1
Clinical and Molecular Characterization of a Novel Homozygo..:
Ha, Zong Yi
;
Chijiwa, Chieko
;
Lewis, Suzanne
Genes. 15 (2024) 4 - p. 461 , 2024
Link:
https://doi.org/10.3390/..
?
2
Genome-wide sequencing and the clinical diagnosis of geneti..:
Elliott, Alison M.
;
Adam, Shelin
;
du Souich, Christèle
...
Human Genetics and Genomics Advances. 3 (2022) 3 - p. 100108 , 2022
Link:
https://doi.org/10.1016/..
?
3
Contribution of Multiple Inherited Variants to Autism Spect..:
Dhaliwal, Jasleen
;
Qiao, Ying
;
Calli, Kristina
...
Genes. 12 (2021) 7 - p. 1053 , 2021
Link:
https://doi.org/10.3390/..
?
4
Aberrant Function of the C-Terminal Tail of HIST1H1E Accele..:
Flex, Elisabetta
;
Martinelli, Simone
;
Van Dijck, Anke
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 493-508 , 2019
Link:
https://doi.org/10.1016/..
?
5
Renpenning syndrome in a female:
Cho, Raymond Y.
;
Peñaherrera, Maria S.
;
Du Souich, Christele
...
American Journal of Medical Genetics Part A. 182 (2019) 3 - p. 498-503 , 2019
Link:
https://doi.org/10.1002/..
?
6
Weaver Syndrome‐Associated EZH2 Protein Variants Show Impai..:
Cohen, Ana S.A.
;
Yap, Damian B.
;
Lewis, M.E. Suzanne
...
Human Mutation. 37 (2016) 3 - p. 301-307 , 2016
Link:
https://doi.org/10.1002/..
?
7
Exome sequencing identifies pathogenic variants of VPS13B i..:
Dastan, Jila
;
Chijiwa, Chieko
;
Tang, Flamingo
...
BMC Medical Genetics. 17 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
8
Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutat..:
Ngai, Ying Fai
;
Chijiwa, Chieko
;
Mercimek‐Mahmutoglu, Saadet
...
American Journal of Medical Genetics Part A. 152A (2010) 11 - p. 2784-2790 , 2010
Link:
https://doi.org/10.1002/..
?
9
Elucidation of a cryptic interstitial 7q31.3 deletion in a ..:
Tyson, Christine
;
McGillivray, Barbara
;
Chijiwa, Chieko
.
American Journal of Medical Genetics Part A. 129A (2004) 3 - p. 254-260 , 2004
Link:
https://doi.org/10.1002/..
?
10
Germline AGO2 mutations impair RNA interference and human n..:
Lessel, Davor
;
Zeitler, Daniela M
;
Reijnders, Margot R F
...
https://research.rug.nl/en/publications/83f39819-c603-41b1-aafb-983f211f5c5e. , 2020
Link:
https://hdl.handle.net/1..
?
11
Germline AGO2 mutations impair RNA interference and human n..:
Lessel, Davor
;
Zeitler, Daniela
;
Reijnders, Margot
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-020-19572-5. , 2020
Link:
https://amu.hal.science/..
?
12
Aberrant function of the C-terminal tail of HIST1H1E Aacele..:
Flex Elisabetta
;
Martinelli Simone
;
Van Dijck Anke
...
info:eu-repo/semantics/altIdentifier/pmid/31447100. , 2019
Link:
http://hdl.handle.net/11..
?
13
Weaver Syndrome-Associated EZH2 Protein Variants Show Impai..:
Cohen, Ana S. A
;
Yap, Damian B
;
Lewis, M. E. Suzanne
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.22946. , 2016
Link:
https://univ-rennes.hal...
?
14
Exome sequencing identifies pathogenic variants of VPS13B i..:
Dastan, Jila
;
Chijiwa, Chieko
;
Tang, Flamingo
...
http://www.biomedcentral.com/1471-2350/17/78. , 2016
Link:
http://www.biomedcentral..
?
15
Weaver Syndrome-Associated EZH2 Protein Variants Show Impai..:
Cohen, Ana S. A
;
Yap, Damian B
;
Lewis, M. E. Suzanne
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.22946. , 2016
Link:
https://univ-rennes.hal...
1-15