Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

By: Thomas, P. QContributor(s): Beddington, R. S. P | Brickman, J. M | Cameron, F | Dattani, M. T | Dunger, D | Forrest, S | Hurst, J | Mcnay, D | Robinson, I. C. A. F | Stanhope, R | Warne, G | Woods, K | Zacharin, MMaterial type: TextTextReference number:PUB10937 In: Human Molecular Genetics 10 (1), 39-45.
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Magazine Magazine Staff publications New Materials Shelf Non-fiction XX(11037.1) (Browse shelf(Opens below)) 1 Available 11037-1001
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