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Issue Date
Title
Author(s)
2014
SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal
Alatzoglou, K.
;
Azriyanti, A.
;
Rogers, N.
;
Ryan, F.
;
Curry, N.
;
Noakes, C.
;
Bignell, P.
;
Hall, G.
;
Littooij, A.
;
Saunders, D.
;
Thomas, P.
;
Stewart, H.
;
Dattani, M.
2001
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia
Thomas, P.
;
Dattani, M.
;
Brickman, J.
;
McNay, D.
;
Warne, G.
;
Zacharin, M.
;
Cameron, F.
;
Hurst, J.
;
Woods, K.
;
Dunger, D.
;
Stanhope, R.
;
Forrest, S.
;
Robinson, I.
;
Beddington, R.
2005
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)
Turton, J.
;
Mehta, A.
;
Raza, J.
;
Woods, K.
;
Tiulpakov, A.
;
Cassar, J.
;
Chong, K.
;
Thomas, P.
;
Eunice, M.
;
Ammini, A.
;
Bouloux, P.
;
Starzyk, J.
;
Hindmarsh, P.
;
Dattani, M.
2005
Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism
Woods, K.
;
Cundall, M.
;
Turton, J.
;
Rizotti, K.
;
Mehta, A.
;
Palmer, R.
;
Wong, J.
;
Chong, W.
;
Al-Zyoud, M.
;
El-Ali, M.
;
Otonkoski, T.
;
Martinez-Barbera, J.P.
;
Thomas, P.
;
Robinson, I.
;
Lovell-Badge, R.
;
Woodward, K.
;
Dattani, M.
Discover
Author
3
Woods, K.
2
Mehta, A.
2
Robinson, I.
2
Turton, J.
1
Al-Zyoud, M.
1
Alatzoglou, K.
1
Ammini, A.
1
Azriyanti, A.
1
Beddington, R.
1
Bignell, P.
.
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Subject
1
Animals
1
Child, Preschool
1
Developmental Disabilities
1
Gene Deletion
1
Hemophilia B
1
Humans
1
Hypopituitarism
1
Hypothalamo-Hypophyseal System
1
Male
1
Mice
.
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Date issued
1
2010 - 2014
3
2001 - 2009