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HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
Published in:
2007
By:
- McNay, David E G;
- Turton, James P;
- Kelberman, Daniel;
- Woods, Kathryn S;
- Brauner, Raja;
- Papadimitriou, Anastasios;
- Keller, Eberhard;
- Keller, Alexandra;
- Haufs, Nele;
- Krude, Heiko;
- Shalet, Stephen M;
- Dattani, Mehul T
Publication type:
journal article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4762, doi. 10.1210/jc.2005-0570
By:
- Turton, James P. G.;
- Reynaud, Rachel;
- Mehta, Ameeta;
- Torpian, John;
- Saveanu, Alexandru;
- Woods, Kathryn S.;
- Tiulpakov, Anatoly;
- Zdravkovic, Vera;
- Hamilton, Jill;
- Attard-Montalto, Simon;
- Parascandalo, Ray;
- Vella, Cecil;
- Clayton, Peter E.;
- Shalet, Stephen;
- Barton, John;
- Brue, Thierry;
- Dattani, Mehul T.
Publication type:
Article
Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 6, p. 4762, doi. 10.1210/jc.2005-0570
By:
- Turton, James P. G.;
- Reynaud, Rachel;
- Mehta, Ameeta;
- Torpiano, John;
- Saveanu, Alexandru;
- Woods, Kathryn S.;
- Tiulpakov, Anatoly;
- Zdravkovic, Vera;
- Hamilton, Jill;
- Attard-Montalto, Simon;
- Parascandalo, Ray;
- Vella, Cecil;
- Clayton, Peter E.;
- Shalet, Stephen;
- Barton, John;
- Brue, Thierry;
- Dattani, Mehul T.
Publication type:
Article
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
Published in:
Clinical Endocrinology, 2005, v. 63, n. 1, p. 10, doi. 10.1111/j.1365-2265.2005.02291.x
By:
- Turton, James P. G.;
- Mehta, Ameeta;
- Raza, Jamal;
- Woods, Kathryn S.;
- Tiulpakov, Anatoly;
- Cassar, Joseph;
- Chong, Kling;
- Thomas, Paul Q.;
- Eunice, Marumudi;
- Ammini, Ariachery C.;
- Bouloux, Pierre M.;
- Starzyk, Jerzy;
- Hindmarsh, Peter C.;
- Dattani, Mehul T.
Publication type:
Article

Found: 4

HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.

Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.

Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).