Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.
Thomas PQ; Dattani MT; Brickman JM; McNay D; Warne G; Zacharin M; Cameron F; Hurst J; Woods K; Dunger D; Stanhope R; Forrest S; Robinson IC; Beddington RS; Human Molecular Genetics, 2001, vol. 10, issue 1, p 39, ISSN 09646906. ISBN 09646906.

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