Skip to main content
Leiden University
Scholarly Publications
Home
Submit
About
Select Collection
All collections
Academic speeches
Dissertations
Faculty of Archaeology
Faculty of Governance and Global Affairs
Faculty of Humanities
Faculty of Science
Faculty of Social and Behavioural Sciences
Leiden Journals, Conference Proceedings and Books
Leiden Law School
Leiden University Press
Medicine / Leiden University Medical Centre (LUMC)
Research output UL
Search box
Your Search
Enabled Filters
(-)
= Davis, T.M.E.
Sort Options
Date (year)
Author / Creator
Title
Refine Results
Resource Type
Article / Letter to editor
(3)
+
-
Availability
Metadata Only
(3)
+
-
Creation Date
2013
(2)
+
-
Faculty
Leiden University Medical Center (LUMC)
(3)
+
-
Collection
Medicine / Leiden University Medical Centre (LUMC)
(3)
+
-
Author
Appelman-Dijkstra, N.M.
(3)
+
-
Bak, B.
(3)
+
-
Beck-Peccoz, P.
(3)
+
-
Bernard, D.J.
(3)
+
-
Biermasz, N.R.
(3)
+
-
Bonomi, M.
(3)
+
-
Breuning, M.H.
(3)
+
-
Campi, I.
(3)
+
-
Chatterjee, K.
(3)
+
-
Corssmit, E.P.
(3)
+
-
Dattani, M.T.
(3)
+
-
Davis, T.M.E.
(3)
+
-
Hennekam, R.C.
(3)
+
-
Oostdijk, W.
(3)
+
-
Pereira, A.M.
(3)
+
-
Persani, L.
(3)
+
-
Schoenmakers, N.
(3)
+
-
Sun, Y.
(3)
+
-
Trotsenburg, A.S.P. van
(3)
+
-
Wit, J.M.
(3)
+
-
Blanco, D.G. del
(2)
+
-
Bosch, C.A.J.
(2)
+
-
Cambridge, E.
(2)
+
-
Dunnen, J.T. den
(2)
+
-
Gharavy, S.N.M.
(2)
+
-
Hokken-Koelega, A.C.S.
(2)
+
-
Hovens, G.C.J.
(2)
+
-
Kant, S.G.
(2)
+
-
Kempers, M.J.
(2)
+
-
Kriek, M.
(2)
+
-
Laros, J.F.J.
(2)
+
-
Martinez-Barbera, J.P.
(2)
+
-
Rangasami, J.J.
(2)
+
-
Ruivenkamp, C.A.L.
(2)
+
-
Stokvis-Brantsma, W.H.
(2)
+
-
Tissier, P. le
(2)
+
-
Voshol, P.
(2)
+
-
Vulsma, T.
(2)
+
-
Wade, M.G.
(2)
+
-
White, J.K.
(2)
+
-
Zhu, H.
(2)
+
-
Show more
Language
en
(3)
+
-
Search results
(1 - 3 of 3)
show grid
show list
save search
The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
Loss-of-function mutations in the immunoglobulin superfamily member 1 gene (IGSF1) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement