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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features
Roessler, E., Du, Y.-Z., Mullor, J. L., Casas, E., Allen, W. P., Gillessen-Kaesbach, G., Roeder, E. R., Ming, J. E., Altaba, A. R. i., Muenke, M.Volume:
100
Language:
english
Journal:
Proceedings of the National Academy of Sciences
DOI:
10.1073/pnas.2235734100
Date:
November, 2003
File:
PDF, 584 KB
english, 2003