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DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyr..:

Peters, C ; Nicholas, AK ; Schoenmakers, E...
https://discovery.ucl.ac.uk/id/eprint/10073520/7/DUOX2DUOXA2%20Mutations%20Frequently%20Cause%20Congenital%20Hypothyroidism%20that%20Evades%20Detection%20on%20Newborn%20Screening%20in%20the%20United%20Ki.pdf. , 2019

Link: https://discovery.ucl.ac.uk/id/eprint/10073520/7/DUOX2..

RT Journal
T1 <Title>DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10073520&Exemplar=1&LAN=DE
				
A1 Peters, C
A1 Nicholas, AK
A1 Schoenmakers, E
A1 Lyons, G
A1 Langham, S
A1 Serra, EG
A1 Sebire, NJ
A1 Muzza, M
A1 Fugazzola, L
A1 Schoenmakers, N
YR 2019
K1 This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0)
K1 which permits unrestricted use
K1 distribution
K1 and reproduction in any medium
K1 provided the original work is properly cited
JF https://discovery.ucl.ac.uk/id/eprint/10073520/7/DUOX2DUOXA2%20Mutations%20Frequently%20Cause%20Congenital%20Hypothyroidism%20that%20Evades%20Detection%20on%20Newborn%20Screening%20in%20the%20United%20Ki.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10073520/7/DUOX2DUOXA2%20Mutations%20Frequently%20Cause%20Congenital%20Hypothyroidism%20that%20Evades%20Detection%20on%20Newborn%20Screening%20in%20the%20United%20Ki.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10073520/7/DUOX2DUOXA2%20Mutations%20Frequently%20Cause%20Congenital%20Hypothyroidism%20that%20Evades%20Detection%20on%20Newborn%20Screening%20in%20the%20United%20Ki.pdf
SF ELIB - SuUB Bremen

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