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
Nephrocalcinosis (enamel renal syndrome) caused by autosoma..:
Jaureguiberry, G
;
De la Dure-Molla, M
;
Parry, D
...
https://discovery.ucl.ac.uk/id/eprint/1388316/1/349989.pdf. , 2012
Link:
https://discovery.ucl.ac.uk/id/eprint/1388316/1/349989..
RT Journal T1
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations
UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:1388316&Exemplar=1&LAN=DE A1 Jaureguiberry, G A1 De la Dure-Molla, M A1 Parry, D A1 Quentric, M A1 Himmerkus, N A1 Koike, T A1 Poulter, J A1 Klootwijk, E A1 Robinette, SL A1 Howie, AJ A1 Patel, V A1 Figueres, ML A1 Stanescu, HC A1 Issler, N A1 Nicholson, JK A1 Bockenhauer, D A1 Laing, C A1 Walsh, SB A1 McCredie, DA A1 Povey, S A1 Asselin, A A1 Picard, A A1 Coulomb, A A1 Medlar, AJ A1 Bailleul-Forestier, I A1 Verloes, A A1 Le Caignec, C A1 Roussey, G A1 Guiol, J A1 Isidor, B A1 Logan, C A1 Shore, R A1 Johnson, C A1 Inglehearn, C A1 Al-Bahlani, S A1 Schmittbuhl, M A1 Clauss, F A1 Huckert, M A1 Laugel, V A1 Ginglinger, E A1 Pajarola, S A1 Spartà, G A1 Bartholdi, D A1 Rauch, A A1 Addor, MC A1 Yamaguti, PM A1 Safatle, HP A1 Acevedo, AC A1 Martelli-Júnior, H A1 dos Santos Netos, PE A1 Coletta, RD A1 Gruessel, S A1 Sandmann, C A1 Ruehmann, D A1 Langman, CB A1 Scheinman, SJ A1 Ozdemir-Ozenen, D A1 Hart, TC A1 Hart, PS A1 Neugebauer, U A1 Schlatter, E A1 Houillier, P A1 Gahl, WA A1 Vikkula, M A1 Bloch-Zupan, A A1 Bleich, M A1 Kitagawa, H A1 Unwin, RJ A1 Mighell, A A1 Berdal, A A1 Kleta, R YR 2012 K1 Adolescent K1 Adult K1 Amelogenesis imperfecta K1 Child K1 Consanguinity K1 Dental enamel proteins K1 Exome K1 Family health K1 Female K1 Genes K1 Recessive K1 Genetic predisposition to disease K1 Genome-wide association study K1 Humans K1 Male K1 Middle aged K1 Mutation K1 Nephrocalcinosis K1 Pedigree K1 Sequence Analysis K1 DNA K1 Syndrome K1 Young Adult JF https://discovery.ucl.ac.uk/id/eprint/1388316/1/349989.pdf LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/1388316/1/349989.pdf DO https://discovery.ucl.ac.uk/id/eprint/1388316/1/349989.pdf SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)