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HESX1: a novel gene implicated in a familial form of septo-optic dysplasia |
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| Authors: | MT Dattani JP Martinez-Barbera PQ Thomas JM Brickman R Gupta JKH Wales PC Hindmarsh RSP Beddington ICAF Robinson |
| Affiliation: | London Centre for Paediatric Endocrinology and Metabolism;Institute of Child Health, London, National Institute for Medical Research;Mill Hill, London, UK, The Murdoch Institute;Melbourne, Australia, and Sheffield Children's Hospital UK |
| Abstract: | |
| Keywords: | HESXl gne homeobox homeodomain missense mutation pituitary Rathke's pouch septo-optic dysplasia |
