C. Hughes
发表
L. Metherell,
L. Guasti,
J. Schimenti,
2012,
The Journal of clinical investigation.
F. Keleştimur,
L. Metherell,
T. Chung,
2010,
The Journal of clinical endocrinology and metabolism.
L. Metherell,
A. Clark,
E. Meimaridou,
2013,
Endocrine development.
M. Dattani,
P. Hindmarsh,
C. Brain,
2022,
Journal of the Endocrine Society.
J. Achermann,
C. Hughes,
E. Man,
2019,
Brook's Clinical Pediatric Endocrinology.
Claire Hughes,
L. Metherell,
L. Guasti,
2013,
Molecular and Cellular Endocrinology.
P. Hindmarsh,
R. Lindsay,
C. Brain,
2018,
Journal of the Endocrine Society.
L. Metherell,
H. Storr,
M. Savage,
2014,
The Journal of clinical endocrinology and metabolism.
Mutations in Nicotinamide Nucleotide Transhydrogenase (NNT) cause familial glucocorticoid deficiency
F. Wagner,
P. Frommolt,
P. Nürnberg,
2012,
Nature Genetics.
L. Metherell,
A. Bereket,
S. Turan,
2011,
The Journal of clinical endocrinology and metabolism.
V. Kimonis,
M. Schneider,
S. Forrester,
2000,
American journal of medical genetics.
L. Metherell,
A. Clark,
C. Hughes,
2009
.
F. Ponchel,
N. Napoli,
P. Pozzilli,
2013,
Diabetologia.
N. S. Thomas,
Michal Ajzensztejn,
Z. Mohamed,
2021,
Egyptian Journal of Medical Human Genetics.
A. Clark,
A. Habeb,
C. Hughes,
2013,
European Journal of Pediatrics.