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Serra, EG
11
results:
Search for persons
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Online (11)
Mediatypes
Articles (Online) (1)
OpenAccess-fulltext (10)
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1
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
Mucosal Immunology. 11 (2018) 2 - p. 562-574 , 2018
Link:
https://doi.org/10.1038/..
?
2
Somatic mosaicism and common genetic variation contribute t..:
Serra, EG
;
Schwerd, T
;
Moutsianas, L
...
https://discovery.ucl.ac.uk/id/eprint/10093033/1/s41467-019-14275-y.pdf. , 2020
Link:
https://discovery.ucl.ac..
?
3
Somatic mosaicism and common genetic variation contribute t..:
Serra, EG
;
Schwerd, T
;
Moutsianas, L
...
NATURE COMMUNICATIONS. , 2020
Link:
https://qmro.qmul.ac.uk/..
?
4
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..
?
5
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
MUCOSAL IMMUNOLOGY. , 2018
Link:
https://qmro.qmul.ac.uk/..
?
6
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
issn:1933-0219. , 2018
Link:
http://hdl.handle.net/11..
?
7
Homozygous loss-of-function mutations in SLC26A7 cause goit..:
Cangul, H
;
Liao, XH
;
Schoenmakers, E
...
JCI insight. , 2018
Link:
https://erepo.uef.fi/han..
?
8
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
https://www.repository.cam.ac.uk/handle/1810/271648. , 2018
Link:
https://www.repository.c..
?
9
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
doi:10.1038/mi.2017.74. , 2017
Link:
https://doi.org/10.1038/..
?
10
NOX1 loss-of-function genetic variants in patients with inf..:
Schwerd, T
;
Bryant, RV
;
Pandey, S
...
https://discovery.ucl.ac.uk/id/eprint/10038829/1/Schwerd_OA%20Rev_mi201774.pdf. , 2017
Link:
https://discovery.ucl.ac..
?
11
Comprehensive Screening of Eight Known Causative Genes in C..:
Nicholas, AK
;
Serra, EG
;
Cangul, H
...
https://discovery.ucl.ac.uk/id/eprint/1532673/1/jc%252E2016-1879.pdf. , 2016
Link:
https://discovery.ucl.ac..
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