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
Häfliger, I.M.
~ 100
results:
Search for persons
X
Format
Online
Print
Mediatypes
Articles (Online)
Bookchapter (Online)
OpenAccess-fulltext
Video (DVD/CD)
Languages
german (1)
english (80)
Sorted by: Relevance
Sorted by: Year
?
1
Multiple independent de novo mutations are associated with ..:
Jacinto, J.G.P.
;
Häfliger, I.M.
;
Letko, A.
...
The Veterinary Journal. 304 (2024) - p. 106069 , 2024
Link:
https://doi.org/10.1016/..
?
2
New genomic features of the polled intersex syndrome varian..:
Simon, R.
;
Lischer, H. E. L.
;
Pieńkowska‐Schelling, A.
...
Animal Genetics. 51 (2020) 3 - p. 439-448 , 2020
Link:
https://doi.org/10.1111/..
?
3
Ear type in sheep is associated with the MSRB3 locus:
Paris, J. M.
;
Letko, A.
;
Häfliger, I. M.
..
Animal Genetics. 51 (2020) 6 - p. 968-972 , 2020
Link:
https://doi.org/10.1111/..
?
4
De novo stop‐lost germline mutation in FGFR3 causes severe ..:
Häfliger, I. M.
;
Letko, A.
;
Murgiano, L.
.
Animal Genetics. 51 (2020) 3 - p. 466-469 , 2020
Link:
https://doi.org/10.1111/..
?
5
A genome‐wide significant association on chromosome 15 for ..:
Hirter, N.
;
Letko, A.
;
Häfliger, I. M.
...
Animal Genetics. 51 (2020) 2 - p. 278-283 , 2020
Link:
https://doi.org/10.1111/..
?
6
Identification of small and large genomic candidate variant..:
Häfliger, I. M.
;
Wiedemar, N.
;
Švara, T.
...
Animal Genetics. 51 (2020) 3 - p. 382-390 , 2020
Link:
https://doi.org/10.1111/..
?
7
A de novo germline mutation of KIT in a white‐spotted Brown..:
Häfliger, I. M.
;
Hirter, N.
;
Paris, J. M.
...
Animal Genetics. 51 (2020) 3 - p. 449-452 , 2020
Link:
https://doi.org/10.1111/..
?
8
Identification of two TYRP1 loss‐of‐function alleles in Val..:
Paris, J. M.
;
Letko, A.
;
Häfliger, I. M.
...
Animal Genetics. 50 (2019) 6 - p. 778-782 , 2019
Link:
https://doi.org/10.1111/..
?
9
A complex structural variant at the KIT locus in cattle wit..:
Küttel, L.
;
Letko, A.
;
Häfliger, I. M.
...
Animal Genetics. 50 (2019) 5 - p. 423-429 , 2019
Link:
https://doi.org/10.1111/..
?
10
An ABCA12 missense variant in a Shorthorn calf with ichthyo..:
Woolley, S. A.
;
Eager, K. L. M.
;
Häfliger, I. M.
...
Animal Genetics. 50 (2019) 6 - p. 749-752 , 2019
Link:
https://doi.org/10.1111/..
?
11
A non‐coding regulatory variant in the 5′‐region of the MIT..:
Hofstetter, S.
;
Seefried, F.
;
Häfliger, I.M.
...
Animal Genetics. 50 (2018) 1 - p. 27-32 , 2018
Link:
https://doi.org/10.1111/..
?
12
Successful trio-based reverse genetic screen in an endanger..:
Häfliger, I. M
;
Seefried, F. R
;
Drögemüller, C
https://boris.unibe.ch/178889/. , 2023
Link:
https://boris.unibe.ch/1..
?
13
A homozygous missense variant in laminin subunit beta 1 as ..:
Jacinto J. G. P
;
Hafliger I. M
;
Bernardini M
...
info:eu-repo/semantics/altIdentifier/wos/WOS:000720318500001. , 2021
Link:
http://hdl.handle.net/11..
?
14
CNGB3 Missense Variant Causes Recessive Achromatopsia in Or..:
Häfliger, I.M
;
Marchionatti, E
;
Stengård, M
...
info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms222212440. , 2021
Link:
https://serval.unil.ch/n..
?
15
A heterozygous missense variant in MAP2K2 in a stillborn ro..:
Jacinto J. G. P
;
Hafliger I. M
;
Gentile A
.
info:eu-repo/semantics/altIdentifier/pmid/34209498. , 2021
Link:
http://hdl.handle.net/11..
1-15