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
Ordóñez-Ugalde, A.
30
results:
Search for persons
X
Format
Online (30)
Mediatypes
Articles (Online) (12)
OpenAccess-fulltext (18)
Languages
english (22)
spanish (4)
Sorted by: Relevance
Sorted by: Year
?
1
Biogeographical origin and timing of the founder ichthyosis..:
Esperón-Moldes, U. S.
;
Pardo-Seco, J.
;
Montalván-Suárez, M.
...
Scientific Reports. 9 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
2
The geographic mosaic of Ecuadorian Y-chromosome ancestry:
Toscanini, U.
;
Gaviria, A.
;
Pardo-Seco, J.
...
Forensic Science International: Genetics. 33 (2018) - p. 59-65 , 2018
Link:
https://doi.org/10.1016/..
?
3
Evaluating the Calling Performance of a Rare Disease NGS Pa..:
Cacheiro, P.
;
Ordóñez-Ugalde, A.
;
Quintáns, B.
...
Molecular Diagnosis & Therapy. 21 (2017) 3 - p. 303-313 , 2017
Link:
https://doi.org/10.1007/..
?
4
Medical genomics: The intricate path from genetic variant i..:
Quintáns, B.
;
Ordóñez-Ugalde, A.
;
Cacheiro, P.
..
Applied & Translational Genomics. 3 (2014) 3 - p. 60-67 , 2014
Link:
https://doi.org/10.1016/..
?
5
Tract-specific damage at spinal cord level in pure heredita..:
Navas-Sánchez, Francisco J.
;
Marcos-Vidal, Luis
;
de Blas, Daniel Martín
...
Journal of Neurology. 269 (2022) 6 - p. 3189-3203 , 2022
Link:
https://doi.org/10.1007/..
?
6
Thalamic atrophy in patients with pure hereditary spastic p..:
Navas-Sánchez, Francisco J.
;
Fernández-Pena, Alberto
;
Martín de Blas, Daniel
...
Journal of Neurology. 268 (2021) 7 - p. 2429-2440 , 2021
Link:
https://doi.org/10.1007/..
?
7
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding ..:
Seixas, Ana I.
;
Loureiro, Joana R.
;
Costa, Cristina
...
The American Journal of Human Genetics. 101 (2017) 1 - p. 87-103 , 2017
Link:
https://doi.org/10.1016/..
?
8
Mutations in the gene encoding PDGF-B cause brain calcifica..:
Keller, Annika
;
Westenberger, Ana
;
Sobrido, Maria J
...
Nature Genetics. 45 (2013) 9 - p. 1077-1082 , 2013
Link:
https://doi.org/10.1038/..
?
9
Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:
Farazi Fard M. A
;
Rebelo A. P
;
Buglo E
...
info:eu-repo/semantics/altIdentifier/pmid/30929741. , 2019
Link:
http://hdl.handle.net/23..
?
10
Biogeographical origin and timing of the founder ichthyosis..:
Esperón-Moldes, U. S
;
Pardo-Seco, J
;
Montalván-Suárez, M
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509209/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
11
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding ..:
Seixas, A
;
Loureiro, R
;
Costa, C
...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501871/pdf/main.pdf. , 2018
Link:
http://hdl.handle.net/10..
?
12
A pentanucleotide ATTTC repeat insertion in the non-coding ..:
Seixas, AI
;
Loureiro, JR
;
Costa, C
...
info:eu-repo/grantAgreement/FCT/5876-PPCDTI/98305/PT. , 2017
Link:
http://hdl.handle.net/10..
?
13
Medical genomics: The intricate path from genetic variant i..:
Quintáns, B
;
Ordóñez-Ugalde, A
;
Cacheiro, P
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887840/. , 2014
Link:
http://www.ncbi.nlm.nih...
?
14
Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:
Farazi Fard, Mohammad Ali
;
Rebelo, Adriana P
;
Buglo, Elena
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557723/. , 2019
Link:
http://www.ncbi.nlm.nih...
?
15
Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:
Farazi Fard, Mohammad Ali
;
Rebelo, Adriana P
;
Buglo, Elena
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451742/. , 2019
Link:
http://www.ncbi.nlm.nih...
1-15
