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Serra, EG
11  Ergebnisse:
Personensuche X
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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/..
 
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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..
 
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3

Somatic mosaicism and common genetic variation contribute t..:

Serra, EG ; Schwerd, T ; Moutsianas, L...
NATURE COMMUNICATIONS.  , 2020
Link: https://qmro.qmul.ac.uk/..
 
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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..
 
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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/..
 
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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..
 
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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..
 
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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..
 
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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/..
 
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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..
 
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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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