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
Mantcheva, Lili
6
results:
Search for persons
X
Format
Online (6)
Mediatypes
Articles (Online) (4)
OpenAccess-fulltext (2)
Sorted by: Relevance
Sorted by: Year
?
1
P535: The undiagnosed rare disease clinic program of Indian..:
Liaqat, Khurram
;
Vetrini, Francesco
;
Conboy, Erin
...
Genetics in Medicine Open. 2 (2024) - p. 101434 , 2024
Link:
https://doi.org/10.1016/..
?
2
Undiagnosed rare disease clinic identifies a novel UBE3A va..:
Bruns, Rebecca
;
Liaqat, Khurram
;
Nasir, Abdul
...
Congenital Anomalies. 64 (2024) 3 - p. 155-160 , 2024
Link:
https://doi.org/10.1111/..
?
3
P433: A novel deep intronic variant in DYNC2H1 characterize..:
Buchh, Muqsit
;
Gillespie, Patrick
;
Treat, Kayla
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100480 , 2023
Link:
https://doi.org/10.1016/..
?
4
A case of MBTPS1‐related disorder due to compound heterozyg..:
Liaqat, Khurram
;
Treat, Kayla
;
Mantcheva, Lili
...
American Journal of Medical Genetics Part A. 194 (2023) 5 - p. , 2023
Link:
https://doi.org/10.1002/..
?
5
Characterization of a novel deep-intronic variant in DYNC2H..:
Buchh, Muqsit
;
Gillespie, Patrick J
;
Treat, Kayla
...
10.1101/mcs.a006254. , 2022
Link:
https://hdl.handle.net/1..
?
6
P433: A novel deep intronic variant in DYNC2H1 characterize..:
Muqsit Buchh
;
Patrick Gillespie
;
Kayla Treat
...
http://www.sciencedirect.com/science/article/pii/S2949774423004806. , 2023
Link:
https://doi.org/10.1016/..
1-6