Search Results - Alatzoglou, K. S

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  1. 1
    SOX3 Deletion in Mouse and Human Is Associated With Persistence of the Craniopharyngeal Canal

    SOX3 Deletion in Mouse and Human Is Associated With Persistence of the Craniopharyngeal Canal by Alatzoglou, K. S, Azriyanti, A, Rogers, N, Ryan, F, Curry, N, Noakes, C, Bignell, P, Hall, G. W, Littooij, A. S, Saunders, D, Thomas, P, Stewart, H, Dattani, M. T

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    Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency

    Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency by Alatzoglou, Kyriaki S., Turton, James P., Kelberman, Daniel, Clayton, Peter E., Mehta, Ameeta, Buchanan, Charles, Aylwin, Simon, Crowne, Elisabeth C., Christesen, Henrik T., Hertel, Niels T., Trainer, Peter J., Savage, Martin O., Raza, Jamal, Banerjee, Kausik, Sinha, Sunil K., Ten, Svetlana, Mushtaq, Talat, Brauner, Raja, Cheetham, Timothy D., Hindmarsh, Peter C., Mullis, Primus E., Dattani, Mehul T.

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