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The Journal of Clinical Endocrinology and Metabolism|August 21, 2014
SOX3 deletion in mouse and human is associated with persistence of the craniopharyngeal canalK S Alatzoglou, A Azriyanti, N Rogers, et al.Human Molecular Genetics|January 4, 2001
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasiaP Q Thomas, M T Dattani, J M Brickman, et al.Nature Genetics|June 10, 1998
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouseM T Dattani, J P Martinez-Barbera, P Q Thomas, et al.Clinical Endocrinology|October 21, 2014
The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarismL C Gregory, C Gaston-Massuet, C L Andoniadou, et al.The Journal of Clinical Endocrinology and Metabolism|October 11, 2013
The IGSF1 deficiency syndrome: characteristics of male and female patientsS D Joustra, N Schoenmakers, L Persani, et al.Pageof 4