I agree that this site is using cookies. You can find further informations
here
.
X
Login
Merkliste (
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
zur Desktop-Version
Toggle navigation
Merkliste
1 Ergebnisse
1
Mutations involving the SRY-related gene SOX8 are associate..:
Portnoi, Marie-France
;
Dumargne, Marie-Charlotte
;
Rojo, Sandra
...
qt41s0n02d. , 2018
Link:
https://escholarship.org/uc/item/41s0n02d
RT Journal T1
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt41s0n02d&Exemplar=1&LAN=DE A1 Portnoi, Marie-France A1 Dumargne, Marie-Charlotte A1 Rojo, Sandra A1 Witchel, Selma F A1 Duncan, Andrew J A1 Eozenou, Caroline A1 Bignon-Topalovic, Joelle A1 Yatsenko, Svetlana A A1 Rajkovic, Aleksandar A1 Reyes-Mugica, Miguel A1 Almstrup, Kristian A1 Fusee, Leila A1 Srivastava, Yogesh A1 Chantot-Bastaraud, Sandra A1 Hyon, Capucine A1 Louis-Sylvestre, Christine A1 Validire, Pierre A1 de Malleray Pichard, Caroline A1 Ravel, Celia A1 Christin-Maitre, Sophie A1 Brauner, Raja A1 Rossetti, Raffaella A1 Persani, Luca A1 Charreau, Eduardo H A1 Dain, Liliana A1 Chiauzzi, Violeta A A1 Mazen, Inas A1 Rouba, Hassan A1 Schluth-Bolard, Caroline A1 MacGowan, Stuart A1 McLean, WH Irwin A1 Patin, Etienne A1 Meyts, Ewa Rajpert-De A1 Jauch, Ralf A1 Achermann, John C A1 Siffroi, Jean-Pierre A1 McElreavey, Ken A1 Bashamboo, Anu PB eScholarship, University of California YR 2018 K1 Rare Diseases K1 Contraception/Reproduction K1 Infertility K1 Clinical Research K1 Genetics K1 Aetiology K1 2.1 Biological and endogenous factors K1 Reproductive health and childbirth K1 46 K1 XX Disorders of Sex Development K1 Adolescent K1 Child K1 Disorder of Sex Development K1 XY K1 Female K1 Humans K1 Male K1 Mutation K1 Missense K1 Oligospermia K1 Primary Ovarian Insufficiency K1 SOXE Transcription Factors K1 Biological Sciences K1 Medical and Health Sciences K1 Genetics & Heredity JF qt41s0n02d LK http://dx.doi.org/https://escholarship.org/uc/item/41s0n02d DO https://escholarship.org/uc/item/41s0n02d SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)